Cas 1208341-63-2,(Z)-methyl 6-(tert-butyldimethylsilyloxy)-3-(phenylthio)hex-2-enoate

1208341-63-2

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Basic information

Product Name: (Z)-methyl 6-(tert-butyldimethylsilyloxy)-3-(phenylthio)hex-2-enoate
Synonyms: (Z)-methyl 6-(tert-butyldimethylsilyloxy)-3-(phenylthio)hex-2-enoate
CAS NO:1208341-63-2
Molecular Formula:
Molecular Weight: 366.597
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)-methyl 6-(tert-butyldimethylsilyloxy)-3-(phenylthio)hex-2-enoate(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-methyl 6-(tert-butyldimethylsilyloxy)-3-(phenylthio)hex-2-enoate(1208341-63-2)
EPA Substance Registry System: (Z)-methyl 6-(tert-butyldimethylsilyloxy)-3-(phenylthio)hex-2-enoate(1208341-63-2)

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: 1208341-63-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1208341-63-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,8,3,4 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1208341-63:
(9*1)+(8*2)+(7*0)+(6*8)+(5*3)+(4*4)+(3*1)+(2*6)+(1*3)=122
122 % 10 = 2
So 1208341-63-2 is a valid CAS Registry Number.

1208341-63-2Upstream product

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1208341-63-2Relevant academic research and scientific papers

Intramolecular Simmons-Smith cyclopropanation. Studies into the reactivity of alkyl-substituted zinc carbenoids, effect of directing groups and synthesis of bicyclo[n.1.0]alkanes

Bull, James A.,Charette, Andre B.

, p. 1895 - 1902 (2010)

An intramolecular Simmons-Smith (IMSS) cyclopropanation has been developed, providing a novel method for the construction of substituted bicycloalkanes. First, functionalized gem-diiodoalkanes containing allylic alcohols were prepared in high yield. Then

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