1-Pyrrolidinecarboxylic acid, 2-(aMinothioxoMethyl)-, 1,1-diMethylethyl ester, (2S)-
(S)-2-THIOCARBAMOYL-PYRROLIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
CAS: 101410-18-8
Molecular Formula: C10H18N2O2S
1-Pyrrolidinecarboxylic acid, 2-(aMinothioxoMethyl)-, 1,1-diMethylethyl ester, (2S)- - Names and Identifiers
1-Pyrrolidinecarboxylic acid, 2-(aMinothioxoMethyl)-, 1,1-diMethylethyl ester, (2S)- - Physico-chemical Properties
| Molecular Formula | C10H18N2O2S |
| Molar Mass | 230.33 |
| Density | 1.191±0.06 g/cm3(Predicted) |
| Melting Point | 195-199 °C(Solv: tetrahydrofuran (109-99-9)) |
| Boling Point | 339.5±52.0 °C(Predicted) |
| pKa | 12.98±0.20(Predicted) |
| Storage Condition | 2-8°C |
1-Pyrrolidinecarboxylic acid, 2-(aMinothioxoMethyl)-, 1,1-diMethylethyl ester, (2S)- - Introduction
N-BOC-thio-L-prolinamide is an organic compound with the following properties:
1. appearance: generally white crystalline or crystalline powder objects.
2. molecular formula: C13H22N2O4S.
3. Molecular weight: 298.39g/mol.
4. melting point: about 182-185 ℃.
N-BOC-thio-L-prolinamide is mainly used as a protecting group (protecting group), usually in the synthesis of peptides or proteins, the amino group of leucine is protected to prevent side reactions in the reaction process. In addition, it can also be used in other organic synthesis reactions.
The preparation of N-BOC-thio-L-prolinamide is usually completed by the following steps:
1. thio-L-prolinamide is reacted with Boc2O (samarium tert-butoxycarbonyl chloride) in an appropriate solvent.
2. After the reaction is completed, the protecting group is usually removed from the product using acidic conditions (such as acetic acid).
Safety precautions when using or handling N-BOC-thio-L-prolinamide:
1. Avoid inhalation, contact with skin or ingestion of the compound. Appropriate protective measures, such as protective gloves, goggles and laboratory external air devices, should be worn.
2. in the operation to avoid contact with strong oxidants and acidic substances, to prevent dangerous reaction.
3. Experiments should be conducted in a well-ventilated environment and follow relevant safety operating procedures.
4. Waste treatment should be carried out in accordance with local chemical waste treatment regulations to avoid environmental pollution.
Please note that before using any chemical, it is important to understand its nature, use and safety information in detail, and to follow appropriate laboratory conditions and procedures.
1. appearance: generally white crystalline or crystalline powder objects.
2. molecular formula: C13H22N2O4S.
3. Molecular weight: 298.39g/mol.
4. melting point: about 182-185 ℃.
N-BOC-thio-L-prolinamide is mainly used as a protecting group (protecting group), usually in the synthesis of peptides or proteins, the amino group of leucine is protected to prevent side reactions in the reaction process. In addition, it can also be used in other organic synthesis reactions.
The preparation of N-BOC-thio-L-prolinamide is usually completed by the following steps:
1. thio-L-prolinamide is reacted with Boc2O (samarium tert-butoxycarbonyl chloride) in an appropriate solvent.
2. After the reaction is completed, the protecting group is usually removed from the product using acidic conditions (such as acetic acid).
Safety precautions when using or handling N-BOC-thio-L-prolinamide:
1. Avoid inhalation, contact with skin or ingestion of the compound. Appropriate protective measures, such as protective gloves, goggles and laboratory external air devices, should be worn.
2. in the operation to avoid contact with strong oxidants and acidic substances, to prevent dangerous reaction.
3. Experiments should be conducted in a well-ventilated environment and follow relevant safety operating procedures.
4. Waste treatment should be carried out in accordance with local chemical waste treatment regulations to avoid environmental pollution.
Please note that before using any chemical, it is important to understand its nature, use and safety information in detail, and to follow appropriate laboratory conditions and procedures.
Last Update：2024-04-10 22:29:15
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Product Name: (S)-tert-Butyl 2-carbamothioylpyrrolidine-1-carboxylate Visit Supplier Webpage Request for quotationCAS: 101410-18-8
Tel: +86-400-900-4166
Email: product@acmec-e.com
Mobile: +86-18621343501
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Product Name: (S)-tert-Butyl 2-carbamothioylpyrrolidine-1-carboxylate Visit Supplier Webpage Request for quotationCAS: 101410-18-8
Tel: +86-18821248368
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Mobile: +86-18821248368
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Product Name: (S)-2-THIOCARBAMOYL-PYRROLIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER Visit Supplier Webpage Request for quotation
CAS: 101410-18-8
Tel: 18301782025
Email: 3008007409@qq.com
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QQ: 3008007409
CAS: 101410-18-8
Tel: 18301782025
Email: 3008007409@qq.com
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View History
1-Pyrrolidinecarboxylic acid, 2-(aMinothioxoMethyl)-, 1,1-diMethylethyl ester, (2S)-
左氧氟沙星-d8
2-((2-氨基乙基)(甲基)氨基)乙酸乙酯二盐酸盐
4-苄基吡啶
7-甲氧基苯并[D]噻唑
1-(3,5-二甲氧基苯基)环丁烷-1-腈
(2-溴乙炔基)三异丙基硅烷
Benzonitrile, 4-[(2-methoxy-3-pyridinyl)carbonyl]-
3-(3-硝基苯基)咪唑啉-2,4-二酮
3,5,6-三氯甲基吡啶
左氧氟沙星-d8
2-((2-氨基乙基)(甲基)氨基)乙酸乙酯二盐酸盐
4-苄基吡啶
7-甲氧基苯并[D]噻唑
1-(3,5-二甲氧基苯基)环丁烷-1-腈
(2-溴乙炔基)三异丙基硅烷
Benzonitrile, 4-[(2-methoxy-3-pyridinyl)carbonyl]-
3-(3-硝基苯基)咪唑啉-2,4-二酮
3,5,6-三氯甲基吡啶