Cas 160255-57-2,(S)-2-[(3-{2-Ethoxycarbonyl-2-[(Z)-hydroxyimino]-ethyl}-1H-indol-4-yl)-methyl-amino]-3-methyl-butyric acid benzyl ester

160255-57-2

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Basic information

Product Name: (S)-2-[(3-{2-Ethoxycarbonyl-2-[(Z)-hydroxyimino]-ethyl}-1H-indol-4-yl)-methyl-amino]-3-methyl-butyric acid benzyl ester
Synonyms:
CAS NO:160255-57-2
Molecular Formula:
Molecular Weight: 465.549
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: (S)-2-[(3-{2-Ethoxycarbonyl-2-[(Z)-hydroxyimino]-ethyl}-1H-indol-4-yl)-methyl-amino]-3-methyl-butyric acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-[(3-{2-Ethoxycarbonyl-2-[(Z)-hydroxyimino]-ethyl}-1H-indol-4-yl)-methyl-amino]-3-methyl-butyric acid benzyl ester(160255-57-2)
EPA Substance Registry System: (S)-2-[(3-{2-Ethoxycarbonyl-2-[(Z)-hydroxyimino]-ethyl}-1H-indol-4-yl)-methyl-amino]-3-methyl-butyric acid benzyl ester(160255-57-2)

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: 160255-57-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 160255-57-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,2,5 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 160255-57:
(8*1)+(7*6)+(6*0)+(5*2)+(4*5)+(3*5)+(2*5)+(1*7)=112
112 % 10 = 2
So 160255-57-2 is a valid CAS Registry Number.

160255-57-2Upstream product

160255-57-2Downstream Products

84590-48-7 indolactam V

160255-57-2Relevant academic research and scientific papers

Protein Kinase C Modulators. Indolactams. 1. Efficient and Flexible Routes for the Preparation of (-)-Indolactam V for Use in the Synthesis of Analogs

Quick, James,Saha, Bijali,Driedger, Paul E.

, p. 8549 - 8552 (2007/10/02)

Three syntheses of the protein kinase C activator, (-)-indolactam V, are described and are compared for their potential utility in the preparation of ILV analogs.In one route the 4-amino functionality is introduced regiospecifically during the constructio

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