142843-22-9

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Basic information

Product Name: L-Histidinamide, N-[(1,1-dimethylethoxy)carbonyl]-L-phenylalanyl-N-[1-(cyclohexylmethyl)- 2-hydroxy-3-[[2-oxo-2-[(1-oxido-1-azabicyclo[2.2.2]oct-3-yl)amino]ethyl] sulfonyl]propyl]-1-[(1,1-dimethylethoxy)carbonyl]-
Synonyms:
CAS NO:142843-22-9
Molecular Formula: C44H67N7O11S
Molecular Weight: 902.122
EINECS: N/A
Product Categories: N/A
Mol File: 142843-22-9.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: L-Histidinamide, N-[(1,1-dimethylethoxy)carbonyl]-L-phenylalanyl-N-[1-(cyclohexylmethyl)- 2-hydroxy-3-[[2-oxo-2-[(1-oxido-1-azabicyclo[2.2.2]oct-3-yl)amino]ethyl] sulfonyl]propyl]-1-[(1,1-dimethylethoxy)carbonyl]-(CAS DataBase Reference)
NIST Chemistry Reference: L-Histidinamide, N-[(1,1-dimethylethoxy)carbonyl]-L-phenylalanyl-N-[1-(cyclohexylmethyl)- 2-hydroxy-3-[[2-oxo-2-[(1-oxido-1-azabicyclo[2.2.2]oct-3-yl)amino]ethyl] sulfonyl]propyl]-1-[(1,1-dimethylethoxy)carbonyl]-(142843-22-9)
EPA Substance Registry System: L-Histidinamide, N-[(1,1-dimethylethoxy)carbonyl]-L-phenylalanyl-N-[1-(cyclohexylmethyl)- 2-hydroxy-3-[[2-oxo-2-[(1-oxido-1-azabicyclo[2.2.2]oct-3-yl)amino]ethyl] sulfonyl]propyl]-1-[(1,1-dimethylethoxy)carbonyl]-(142843-22-9)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 142843-22-9(Hazardous Substances Data)

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L-Histidinamide, N-[(1,1-dimethylethoxy)carbonyl]-L-phenylalanyl-N-[1-(cyclohexylmethyl)- 2-hydroxy-3-[[2-oxo-2-[(1-oxido-1-azabicyclo[2.2.2]oct-3-yl)amino]ethyl] sulfonyl]propyl]-1-[(1,1-dimethyletho
Cas No: 142843-22-9
USD $ 100.0-100.0 / Gram
10 Gram
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Zibo Hangyu Biotechnology Development Co., Ltd
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L-Histidinamide, N-[(1,1-dimethylethoxy)carbonyl]-L-phenylalanyl-N-[1-(cyclohexylmethyl)- 2-hydroxy-3-[[2-oxo-2-[(1-oxido-1-azabicyclo[2.2.2]oct-3-yl)amino]ethyl] sulfonyl]propyl]-1-[(1,1-dimethyletho
Cas No: 142843-22-9
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Kono Chem Co.,Ltd
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142843-22-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 142843-22-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,8,4 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 142843-22:
(8*1)+(7*4)+(6*2)+(5*8)+(4*4)+(3*3)+(2*2)+(1*2)=119
119 % 10 = 9
So 142843-22-9 is a valid CAS Registry Number.

142843-22-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name	4-((S)-2-((S)-2-tert-Butoxycarbonylamino-3-phenyl-propionylamino)-2-{(1S,2R)-1-cyclohexylmethyl-2-hydroxy-3-[(1-oxy-1-aza-bicyclo[2.2.2]oct-3-ylcarbamoyl)-methanesulfonyl]-propylcarbamoyl}-ethyl)-imidazole-1-carboxylic acid tert-butyl ester

1.2 Other means of identification

Product number	-
Other names	-

1.3 Recommended use of the chemical and restrictions on use

Identified uses	For industry use only.
Uses advised against	no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number	-
Service hours	Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:142843-22-9 SDS

142843-22-9Upstream product

142843-22-9Downstream Products

143396-51-4 {(S)-1-[(S)-1-{(1S,2R)-1-Cyclohexylmethyl-2-hydroxy-3-[(1-oxy-1-aza-bicyclo[2.2.2]oct-3-ylcarbamoyl)-methanesulfonyl]-propylcarbamoyl}-2-(1H-imidazol-4-yl)-ethylcarbamoyl]-2-phenyl-ethyl}-carbamic acid tert-butyl ester

142843-22-9Relevant articles and documents

Inhibitors of Human Renin with C-Termini Derived from Amides and Esters of α-Mercaptoalkanoic Acids

Ashton, Wallace T.,Cantone, Christine L.,Tolman, Richard L.,Greenlee, William J.,Lynch, Robert J.,et al.

, p. 2772 - 2781 (2007/10/02)

New transition-state analogues bearing C-termini derived from α-mercaptoalkanoic acids, esters, and amides were prepared and evaluated as inhibitors of human renin.Addition of α-mercaptoalkanoate esters to a chiral Boc-amino epoxide intermediate led ultim

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