Cas 934008-60-3,(Z)-6-((2R,5R,8R,11R,12S)-8-benzyl-2-isopropyl-5,12-dimethyl-3,6,9,13-tetraoxo-1,4,7,10-tetraaza-cyclotridec-11-yl)-hex-4-enioc acid 2,2,2-trichloro-ethyl ester

934008-60-3

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Basic information

Product Name: (Z)-6-((2R,5R,8R,11R,12S)-8-benzyl-2-isopropyl-5,12-dimethyl-3,6,9,13-tetraoxo-1,4,7,10-tetraaza-cyclotridec-11-yl)-hex-4-enioc acid 2,2,2-trichloro-ethyl ester
Synonyms: (Z)-6-((2R,5R,8R,11R,12S)-8-benzyl-2-isopropyl-5,12-dimethyl-3,6,9,13-tetraoxo-1,4,7,10-tetraaza-cyclotridec-11-yl)-hex-4-enioc acid 2,2,2-trichloro-ethyl ester
CAS NO:934008-60-3
Molecular Formula:
Molecular Weight: 646.011
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: (Z)-6-((2R,5R,8R,11R,12S)-8-benzyl-2-isopropyl-5,12-dimethyl-3,6,9,13-tetraoxo-1,4,7,10-tetraaza-cyclotridec-11-yl)-hex-4-enioc acid 2,2,2-trichloro-ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-6-((2R,5R,8R,11R,12S)-8-benzyl-2-isopropyl-5,12-dimethyl-3,6,9,13-tetraoxo-1,4,7,10-tetraaza-cyclotridec-11-yl)-hex-4-enioc acid 2,2,2-trichloro-ethyl ester(934008-60-3)
EPA Substance Registry System: (Z)-6-((2R,5R,8R,11R,12S)-8-benzyl-2-isopropyl-5,12-dimethyl-3,6,9,13-tetraoxo-1,4,7,10-tetraaza-cyclotridec-11-yl)-hex-4-enioc acid 2,2,2-trichloro-ethyl ester(934008-60-3)

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: 934008-60-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 934008-60-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,4,0,0 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 934008-60:
(8*9)+(7*3)+(6*4)+(5*0)+(4*0)+(3*8)+(2*6)+(1*0)=153
153 % 10 = 3
So 934008-60-3 is a valid CAS Registry Number.

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934008-60-3Relevant academic research and scientific papers

Total synthesis of azumamide A and azumamide E, evaluation as histone deacetylase inhibitors, and design of a more potent analogue

Wen, Shijun,Carey, Krystle L.,Nakao, Yoichi,Fusetani, Nobuhiro,Packham, Graham,Ganesan

, p. 1105 - 1108 (2007)

(Chemical Equation Presented) The unprecedented diastereoselective Mannich reaction of a Z-allylsulfoximine was a key step in the total synthesis of the marine natural products azumamide A and E, and an unnatural analogue. Their relative potency as histone deacetylase inhibitors was evaluated and found to correlate with predicted zinc-binding affinity.

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