Cas 91852-06-1,1H-Imidazole-1-carboxylic acid, 4-[2-[[(1,1-dimethylethoxy)carbonyl]amino]-4-(trimethylsilyl)-3-butynyl]-2- (phenylthio)-, 1,1-dimethylethyl ester

91852-06-1

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Basic information

Product Name: 1H-Imidazole-1-carboxylic acid, 4-[2-[[(1,1-dimethylethoxy)carbonyl]amino]-4-(trimethylsilyl)-3-butynyl]-2- (phenylthio)-, 1,1-dimethylethyl ester
Synonyms:
CAS NO:91852-06-1
Molecular Formula: C26H37N3O4SSi
Molecular Weight: 515.749
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-Imidazole-1-carboxylic acid, 4-[2-[[(1,1-dimethylethoxy)carbonyl]amino]-4-(trimethylsilyl)-3-butynyl]-2- (phenylthio)-, 1,1-dimethylethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 1H-Imidazole-1-carboxylic acid, 4-[2-[[(1,1-dimethylethoxy)carbonyl]amino]-4-(trimethylsilyl)-3-butynyl]-2- (phenylthio)-, 1,1-dimethylethyl ester(91852-06-1)
EPA Substance Registry System: 1H-Imidazole-1-carboxylic acid, 4-[2-[[(1,1-dimethylethoxy)carbonyl]amino]-4-(trimethylsilyl)-3-butynyl]-2- (phenylthio)-, 1,1-dimethylethyl ester(91852-06-1)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 91852-06-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 91852-06-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,8,5 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 91852-06:
(7*9)+(6*1)+(5*8)+(4*5)+(3*2)+(2*0)+(1*6)=141
141 % 10 = 1
So 91852-06-1 is a valid CAS Registry Number.

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91852-06-1Relevant academic research and scientific papers

SYTHESIS OF α-ETHYNYLHISTAMINE, AN INACTIVATOR OF HISTITDINE DECARBOXYLASE

Holbert, Gene W.,Metcalf, Brian W.

, p. 1141 - 1144 (2007/10/02)

α-ethynylhistamine, an inactivator of histidine decarboxylase, has been synthesized via addition of the t-butyl N-trimethylsilyl-prop-2-ynylcarbamate dianion to epibromohydrin to afford the epoxide 6. 6 was converted to the corresponding bromoketone 8 whi

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