N-BOC-5-溴吲哚-2-硼酸1-(叔丁氧羰基-5-溴-1H-吲哚-2-基)硼酸

N-BOC-5-溴吲哚-2-硼酸1-(叔丁氧羰基-5-溴-1H-吲哚-2-基)硼酸 - Names and Identifiers

Name	1-N-Boc-5-bromoindole-2-boronic acid
Synonyms	1-BOC-5-BROMOINDOLE-2-BORONIC ACID N-Boc-5-bromoindole-2-boronic acid 1-BOC-5-BROMO-2-INDOLEBORONIC ACID 1-N-Boc-5-bromoindole-2-boronic acid N-(Boc-5-bromo-2-indolyl)boronic acid 1-BOC-5-BROMO-1H-INDOLE-2-BORONIC ACID 5-bromo-1-t-butoxycarbonylindole-2-boronic acid 5-Bromo-1-(tert-butoxycarbonyl)-1H-indol-2-ylboronic acid [5-Bromo-1-(tert-butoxycarbonyl)-1H-indol-2-yl]boronic acid 2-Borono-5-bromo-1H-indole-1-carboxylic acid tert-butyl ester 1H-Indole-1-carboxylic acid, 2-borono-5-bromo-, 1,1-dimethylethyl ester
CAS	475102-13-7
InChI	InChI=1/C13H15BBrNO4/c1-13(2,3)20-12(17)16-10-5-4-9(15)6-8(10)7-11(16)14(18)19/h4-7,18-19H,1-3H3

N-BOC-5-溴吲哚-2-硼酸1-(叔丁氧羰基-5-溴-1H-吲哚-2-基)硼酸 - Physico-chemical Properties

Molecular Formula	C13H15BBrNO4
Molar Mass	339.98
Density	1.45
Melting Point	93 °C
Boling Point	488.3°C at 760 mmHg
Flash Point	249.1°C
Vapor Presure	2.39E-10mmHg at 25°C
Appearance	Solid
Storage Condition	Keep Cold
Refractive Index	1.576
MDL	MFCD03701683

N-BOC-5-溴吲哚-2-硼酸1-(叔丁氧羰基-5-溴-1H-吲哚-2-基)硼酸 - Risk and Safety

Risk Codes	R20/21/22 - Harmful by inhalation, in contact with skin and if swallowed. R36/37/38 - Irritating to eyes, respiratory system and skin.
Safety Description	S22 - Do not breathe dust. S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.
WGK Germany	3
HS Code	29310095
Hazard Note	Irritant

N-BOC-5-溴吲哚-2-硼酸1-(叔丁氧羰基-5-溴-1H-吲哚-2-基)硼酸 - Introduction

Acid is an organic compound that contains the Boron (boron) and Bromoindole (bromoindole) groups in its chemical structure.

nature, acid is a white to light yellow solid, stable at room temperature. It has low solubility in water and is more suitable for use in organic solvents. The compound can be characterized by nuclear magnetic resonance (NMR) and mass spectrometry (MS).

In terms of use, acid is often used as an important intermediate in organic synthesis reactions. It can participate in SuZ-solid phase reaction, Suzuki-Miyaura coupling reaction, etc., and is used to synthesize compounds with indole and boronic acid functional groups. These compounds have important biological activities in the field of medicine and can be used in pharmaceutical research and drug development.

In terms of preparation, the synthesis of acid usually includes a multi-step reaction. First, brominated indole reacts with boronic acid to form 5-bromoindole-2-boronic acid. Next, by chemical reaction with N-tert-butyloxycarbonyl (N-Boc), the N-Boc group is introduced into the target molecule to obtain the final product P acid.

in terms of safety information, acid specific safety information may lack specific information, so the use should follow the laboratory safety practice. In addition, for the use of any chemical substances, it is recommended that users wear personal protective equipment necessary for the laboratory and operate under appropriate conditions to avoid direct contact with skin, eyes or food. Consult chemical suppliers or relevant safety databases for more detailed safety information when required.

Last Update：2024-04-10 22:30:50

N-BOC-5-溴吲哚-2-硼酸1-(叔丁氧羰基-5-溴-1H-吲哚-2-基)硼酸

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CAS: 475102-13-7
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