Cas 1026818-81-4,[(S)-2-Methyl-1-(1-methyl-1H-benzoimidazole-2-carbonyl)-propyl]-carbamic acid benzyl ester

1026818-81-4

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Basic information

Product Name: [(S)-2-Methyl-1-(1-methyl-1H-benzoimidazole-2-carbonyl)-propyl]-carbamic acid benzyl ester
Synonyms:
CAS NO:1026818-81-4
Molecular Formula:
Molecular Weight: 365.432
EINECS: N/A
Product Categories: N/A
Mol File: 1026818-81-4.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: [(S)-2-Methyl-1-(1-methyl-1H-benzoimidazole-2-carbonyl)-propyl]-carbamic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [(S)-2-Methyl-1-(1-methyl-1H-benzoimidazole-2-carbonyl)-propyl]-carbamic acid benzyl ester(1026818-81-4)
EPA Substance Registry System: [(S)-2-Methyl-1-(1-methyl-1H-benzoimidazole-2-carbonyl)-propyl]-carbamic acid benzyl ester(1026818-81-4)

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: 1026818-81-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1026818-81-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,6,8,1 and 8 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1026818-81:
(9*1)+(8*0)+(7*2)+(6*6)+(5*8)+(4*1)+(3*8)+(2*8)+(1*1)=144
144 % 10 = 4
So 1026818-81-4 is a valid CAS Registry Number.

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1026818-81-4Relevant articles and documents

Peptidyl α-Ketoheterocyclic Inhibitors of Human Neutrophil Elastase. 2. Effect of Varying the Heterocyclic Ring on in Vitro Potency

Edwards, Philip D.,Wolanin, Donald J.,Andisik, Donald W.,Davis, Watthew W.

, p. 76 - 85 (2007/10/02)

A series of peptidyl α-ketoheterocycles were synthesized and evaluated for their in vitro inhibition of human neutrophil elastase (HNE).Several heterocycles, including oxazoline and benzoxazole, afforded extremely potent inhibitors of HNE (1p-r) with nano

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