Cas 248931-01-3,(2RS,3R)-3-amino-N-(4-chloro-2,5-dimethoxyphenyl)-4-cyclohexyl-2-hydroxybutanamide hydrochloride

248931-01-3

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Basic information

Product Name: (2RS,3R)-3-amino-N-(4-chloro-2,5-dimethoxyphenyl)-4-cyclohexyl-2-hydroxybutanamide hydrochloride
Synonyms:
CAS NO:248931-01-3
Molecular Formula:
Molecular Weight: 407.337
EINECS: N/A
Product Categories: N/A

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: (2RS,3R)-3-amino-N-(4-chloro-2,5-dimethoxyphenyl)-4-cyclohexyl-2-hydroxybutanamide hydrochloride(CAS DataBase Reference)
NIST Chemistry Reference: (2RS,3R)-3-amino-N-(4-chloro-2,5-dimethoxyphenyl)-4-cyclohexyl-2-hydroxybutanamide hydrochloride(248931-01-3)
EPA Substance Registry System: (2RS,3R)-3-amino-N-(4-chloro-2,5-dimethoxyphenyl)-4-cyclohexyl-2-hydroxybutanamide hydrochloride(248931-01-3)

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: 248931-01-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 248931-01-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,8,9,3 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 248931-01:
(8*2)+(7*4)+(6*8)+(5*9)+(4*3)+(3*1)+(2*0)+(1*1)=153
153 % 10 = 3
So 248931-01-3 is a valid CAS Registry Number.

248931-01-3Upstream product

248931-01-3Downstream Products

248931-01-3Relevant academic research and scientific papers

Substituted β-amino acid inhibitors of methionine aminopeptidase-2

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, (2008/06/13)

A class of substituted b-amino acids are potent inhibitor of methionine aminopeptidase type 2 (MetAP2) and are thus useful in inhibiting angiogenesis and disease conditions which depend upon angiogenesis for their development such as diabetic retinopathy, tumor growth, and conditions of inflammation. Pharmaceutical compounds containing the compounds and methods of inhibiting methionine aminopeptidase-2, and angiogenesis are also disclosed.

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