Cas 88549-15-9,1H-Benzimidazole-2-propanoic acid, 5,6-dichloro-a-[[(phenylmethoxy)carbonyl]amino]-, phenylmethyl ester, (R)-

88549-15-9

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Basic information

Product Name: 1H-Benzimidazole-2-propanoic acid, 5,6-dichloro-a-[[(phenylmethoxy)carbonyl]amino]-, phenylmethyl ester, (R)-
Synonyms:
CAS NO:88549-15-9
Molecular Formula: C25H21Cl2N3O4
Molecular Weight: 498.365
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: 1H-Benzimidazole-2-propanoic acid, 5,6-dichloro-a-[[(phenylmethoxy)carbonyl]amino]-, phenylmethyl ester, (R)-(CAS DataBase Reference)
NIST Chemistry Reference: 1H-Benzimidazole-2-propanoic acid, 5,6-dichloro-a-[[(phenylmethoxy)carbonyl]amino]-, phenylmethyl ester, (R)-(88549-15-9)
EPA Substance Registry System: 1H-Benzimidazole-2-propanoic acid, 5,6-dichloro-a-[[(phenylmethoxy)carbonyl]amino]-, phenylmethyl ester, (R)-(88549-15-9)

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: 88549-15-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 88549-15-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,5,4 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 88549-15:
(7*8)+(6*8)+(5*5)+(4*4)+(3*9)+(2*1)+(1*5)=179
179 % 10 = 9
So 88549-15-9 is a valid CAS Registry Number.

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88549-15-9Relevant academic research and scientific papers

Synthesis of a novel class of heteroaromatic amino acids and their use in the preparation of analogues of luteinizing hormone-releasing hormone

Nestor Jr.,Horner,Ho,Jones,McRae,Vickery

, p. 320 - 325 (2007/10/02)

A novel class of heterocyclic aromatic amino acids based on the 3-(2-benzimidazolyl)alanine system has been generated by chiral synthesis from D- or L-aspartic acid. The use of variously substituted o-phenylenediamines for condensation with the β-carboxyl

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