80745-09-1 - Names and Identifiers
Name | N(A)-Z-N(O)-(4-methoxy-2,3,6-trime.benz-enesulf.)-L-arg ca S
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Synonyms | cyclohexanamine Z-Arg(Mtr)-Oh Cha Z-Arg(Mtr)-OH·CHA Z-Arg(Mtr)-OH*CHA Z-Arg(Mtr)-OH.CHA Z-ARG(MTR)-OH CHA CBZ-Arg(Mtr)-OH·CHA Z-Arg(Mtr)-OH cyclohexylamine salt Z-Arg(Mtr)-OH cyclohexylammonium salt N(A)-Z-N(O)-(4-methoxy-2,3,6-trime.benz-enesulf.)-L-arg ca S Z-Arg(Mtr)-OH·CHA N-α-Z-N-ω-4-Methoxy-2,3,6-triMethyl benze- N-Cbz-N'-(4-Methoxy-2,3,6-trimethylbenzenesulfonyl)-L-arginine cyclohexylammonium salt Nα-Z-Nω-(4-methoxy-2,3,6-trimethylbenzenesulfonyl)-L-arginine cyclohexylammonium salt N-alpha-Cbz-N-omega-(4-methoxy-2,3,6-trimethylbenzenesulfonyl)-L-arginine cyclohexylamine (2S)-2-benzyloxycarbonylamino-5-[[N-(4-methoxy-2,3,6-trimethyl-phenyl)sulfonylcarbamimidoyl]amino]pentanoic acid cyclohexanamine (S)-2-(benzyloxycarbonylamino)-5-(3-(4-methoxy-2,3,6-trimethylphenylsulfonyl)guanidino)pentanoate
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CAS | 80745-09-1
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InChI | InChI=1/C24H32N4O7S.C6H13N/c1-15-13-20(34-4)16(2)17(3)21(15)36(32,33)28-23(25)26-12-8-11-19(22(29)30)27-24(31)35-14-18-9-6-5-7-10-18;7-6-4-2-1-3-5-6/h5-7,9-10,13,19H,8,11-12,14H2,1-4H3,(H,27,31)(H,29,30)(H3,25,26,28);6H,1-5,7H2/t19-;/m0./s1 |
80745-09-1 - Physico-chemical Properties
Molecular Formula | C30H45N5O7S
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Molar Mass | 619.77 |
Melting Point | 196-199°C |
Boling Point | 801.6°C at 760 mmHg |
Flash Point | 438.6°C |
Vapor Presure | 4.07E-27mmHg at 25°C |
BRN | 5713370 |
Storage Condition | Inert atmosphere,Room Temperature |
80745-09-1 - Risk and Safety
WGK Germany | 3 |
FLUKA BRAND F CODES | 10-21 |
80745-09-1 - Introduction
N(A)-Z-N(O)-(4-methoxy-2,3,6-trime.benz-enesulf.)-L-arg ca S is a compound that can be abbreviated as N(A)-Z-N(O)-(4-methoxy-2,3,6-trime.benz-enesulf.)-L-arg ca S.
Properties: This compound is a solid with a white or off-white color. It is relatively stable at room temperature and has good solubility.
application: N(A)-Z-N(O)-(4-methoxy-2,3,6-trime.benz-enesulf.)-L-arg ca S is commonly used as a protecting group in chemical synthesis. It can protect the amino and carboxyl groups in L-arginine and prevent side reactions under specific reaction conditions.
preparation method: the synthesis of N(A)-Z-N(O)-(4-methoxy-2,3,6-trime.benz-enesulf.)-L-arg ca S usually requires a series of chemical steps. Briefly, N(A)-Z-L-arginine is first reacted with 4-methoxy-2,3,6-trimethylbenzenesulfonyl chloride to give the intermediate N(A)-Z-N(O)-(4-methoxy-2,3,6-trime.benz-enesulf.)-L-arg. This intermediate was then reacted with hydrochloric acid to give the final product N(A)-Z-N(O)-(4-methoxy-2,3,6-trime.benz-enesulf.)-L-arg ca S.
safety information: N(A)-Z-N(O)-(4-methoxy-2,3,6-trime.benz-enesulf.)-for specific safety information L-arg ca S, refer to the safety data sheets of relevant chemicals. When handling and using compounds, follow correct laboratory procedures, wear personal protective equipment, and avoid direct contact with skin and eyes. If you come into contact with the compound, rinse immediately with plenty of water and seek medical help.
Last Update:2024-04-09 15:18:00