2-(Tert-Butoxycarbonyl)-1,2,3,4-Tetrahydroisoquinoline-6-Carboxylic Acid
2-(Tert-Butoxycarbonyl)-1,2,3,4-Tetrahydroisoquinoline-6-Carboxylic Acid
CAS: 170097-67-3
Molecular Formula: C15H19NO4
2-(Tert-Butoxycarbonyl)-1,2,3,4-Tetrahydroisoquinoline-6-Carboxylic Acid - Names and Identifiers
2-(Tert-Butoxycarbonyl)-1,2,3,4-Tetrahydroisoquinoline-6-Carboxylic Acid - Physico-chemical Properties
| Molecular Formula | C15H19NO4 |
| Molar Mass | 277.32 |
| Density | 1?+-.0.06 g/cm3(Predicted) |
| Boling Point | 429.3±45.0 °C(Predicted) |
| Flash Point | 213.4°C |
| Vapor Presure | 3.93E-08mmHg at 25°C |
| pKa | 4.33±0.20(Predicted) |
| Storage Condition | 2-8°C |
| Refractive Index | 1.563 |
2-(Tert-Butoxycarbonyl)-1,2,3,4-Tetrahydroisoquinoline-6-Carboxylic Acid - Introduction
2-(Tert-Butoxycarbonyl)-1,2,3, Acid is an organic compound that contains the Boc Group (t-butoxycarbonylaminomethyl) in its chemical structure. The following is an introduction to its nature, use, preparation and safety information:
Nature:
2-(Tert-Butoxycarbonyl)-1,2,3, Acid is a solid with a white to light yellow color. It is stable at room temperature, but will decompose under high temperature, strong acid and strong alkali conditions.
Use:
2-(Tert-Butoxycarbonyl)-1,2,3, Acid is often used as a protecting group (Boc protecting group) in organic chemical synthesis. It can be reacted with an amino compound to form a N-Boc protected amino compound. Such a protecting group can protect the amino group without interfering with other functional groups, allowing other parts of the molecule to undergo chemical reactions. It has a wide range of applications, including drug synthesis, multi-step organic synthesis and natural product synthesis.
Method:
2-(Tert-Butoxycarbonyl)-1,2,3, Acid is usually prepared by organic synthesis methods. One common method is to react N-Boc-aminocarbols with certain ring complexing reagents such as cyclopentadienyl diruthenium linkages (Cp2RuCl). The resulting intermediate is further reacted with 1,2,3,4-tetrahydroisoquinoline to give the desired product.
Safety Information:
2-(Tert-Butoxycarbonyl)-1,2,3, the use of Acid should pay attention to the following points:
1. It is a combustible material, to avoid contact with high temperature, flame and oxidant.
2. During use, be careful to avoid inhalation, contact with skin and eyes, and use personal protective equipment such as gloves, glasses and protective clothing when necessary.
3. During storage and handling, appropriate safety measures should be observed to avoid its leakage into the environment, and relevant laws and regulations should be observed.
Nature:
2-(Tert-Butoxycarbonyl)-1,2,3, Acid is a solid with a white to light yellow color. It is stable at room temperature, but will decompose under high temperature, strong acid and strong alkali conditions.
Use:
2-(Tert-Butoxycarbonyl)-1,2,3, Acid is often used as a protecting group (Boc protecting group) in organic chemical synthesis. It can be reacted with an amino compound to form a N-Boc protected amino compound. Such a protecting group can protect the amino group without interfering with other functional groups, allowing other parts of the molecule to undergo chemical reactions. It has a wide range of applications, including drug synthesis, multi-step organic synthesis and natural product synthesis.
Method:
2-(Tert-Butoxycarbonyl)-1,2,3, Acid is usually prepared by organic synthesis methods. One common method is to react N-Boc-aminocarbols with certain ring complexing reagents such as cyclopentadienyl diruthenium linkages (Cp2RuCl). The resulting intermediate is further reacted with 1,2,3,4-tetrahydroisoquinoline to give the desired product.
Safety Information:
2-(Tert-Butoxycarbonyl)-1,2,3, the use of Acid should pay attention to the following points:
1. It is a combustible material, to avoid contact with high temperature, flame and oxidant.
2. During use, be careful to avoid inhalation, contact with skin and eyes, and use personal protective equipment such as gloves, glasses and protective clothing when necessary.
3. During storage and handling, appropriate safety measures should be observed to avoid its leakage into the environment, and relevant laws and regulations should be observed.
Last Update：2024-04-09 02:00:43
Supplier List
Spot supply
Product Name: 2-(tert-Butoxycarbonyl)-1,2,3,4-tetrahydroisoquinoline-6-carboxylic acid Visit Supplier Webpage Request for quotationCAS: 170097-67-3
Tel: +86-400-900-4166
Email: product@acmec-e.com
Mobile: +86-18621343501
QQ: 2881950922
Wechat: 18621343501
WhatsApp: +86-18621343501
Spot supply
Product Name: 2-(tert-Butoxycarbonyl)-1,2,3,4-tetrahydroisoquinoline-6-carboxylic acid Visit Supplier Webpage Request for quotationCAS: 170097-67-3
Tel: +86-18821248368
Email: Int06@meryer.com
Mobile: +86-18821248368
QQ: 495145328
WhatsApp: +86-18821248368
Product Name: 2-(TERT-BUTOXYCARBONYL)-1,2,3,4-TETRAHYDROISOQUINOLINE-6-CARBOXYLIC ACID Visit Supplier Webpage Request for quotation
CAS: 170097-67-3
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
CAS: 170097-67-3
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Spot supply
Product Name: 2-(tert-Butoxycarbonyl)-1,2,3,4-tetrahydroisoquinoline-6-carboxylic acid Visit Supplier Webpage Request for quotationCAS: 170097-67-3
Tel: +86-400-900-4166
Email: product@acmec-e.com
Mobile: +86-18621343501
QQ: 2881950922
Wechat: 18621343501
WhatsApp: +86-18621343501
Spot supply
Product Name: 2-(tert-Butoxycarbonyl)-1,2,3,4-tetrahydroisoquinoline-6-carboxylic acid Visit Supplier Webpage Request for quotationCAS: 170097-67-3
Tel: +86-18821248368
Email: Int06@meryer.com
Mobile: +86-18821248368
QQ: 495145328
WhatsApp: +86-18821248368
Product Name: 2-(TERT-BUTOXYCARBONYL)-1,2,3,4-TETRAHYDROISOQUINOLINE-6-CARBOXYLIC ACID Visit Supplier Webpage Request for quotation
CAS: 170097-67-3
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
CAS: 170097-67-3
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
View History
2-(Tert-Butoxycarbonyl)-1,2,3,4-Tetrahydroisoquinoline-6-Carboxylic Acid
5-(2-aminopropyl)-2,3-dihydro-1H-indene
50505-80-1
2-{[5-benzyl-4-(4-methoxyphenyl)-4H-1,2,4-triazol-3-yl]sulfanyl}-N,N-diphenylacetamide
3-Bromo-N-(3-chloropropyl)benzenesulphonamide 97%
2-[(1R)-1-(2,4,5-Trimethoxyphenyl)-2-propenyl]phenol
1,3-Dioxo-2-(4-[1,2,4]triazol-1-ylmethyl-phenyl)-2,3-dihydro-1H-isoindole-5-carboxylic acid
7-amino 3-oxymethyl-3-cephem -4-carboxylic acid
2-(t-Butoxycarbonyl)ethylboronic acid,pinacol ester
314245-33-5
5-(2-aminopropyl)-2,3-dihydro-1H-indene
50505-80-1
2-{[5-benzyl-4-(4-methoxyphenyl)-4H-1,2,4-triazol-3-yl]sulfanyl}-N,N-diphenylacetamide
3-Bromo-N-(3-chloropropyl)benzenesulphonamide 97%
2-[(1R)-1-(2,4,5-Trimethoxyphenyl)-2-propenyl]phenol
1,3-Dioxo-2-(4-[1,2,4]triazol-1-ylmethyl-phenyl)-2,3-dihydro-1H-isoindole-5-carboxylic acid
7-amino 3-oxymethyl-3-cephem -4-carboxylic acid
2-(t-Butoxycarbonyl)ethylboronic acid,pinacol ester
314245-33-5