Cas 1160615-46-2,(1R,2R,3R)-1-methoxycarbonyl-trans-2-(4-bromophenyl)-cis-3-[(E)-2-(trimethylsilyl)vinyl]cyclopropane

1160615-46-2

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Basic information

Product Name: (1R,2R,3R)-1-methoxycarbonyl-trans-2-(4-bromophenyl)-cis-3-[(E)-2-(trimethylsilyl)vinyl]cyclopropane
Synonyms: (1R,2R,3R)-1-methoxycarbonyl-trans-2-(4-bromophenyl)-cis-3-[(E)-2-(trimethylsilyl)vinyl]cyclopropane
CAS NO:1160615-46-2
Molecular Formula:
Molecular Weight: 353.331
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: (1R,2R,3R)-1-methoxycarbonyl-trans-2-(4-bromophenyl)-cis-3-[(E)-2-(trimethylsilyl)vinyl]cyclopropane(CAS DataBase Reference)
NIST Chemistry Reference: (1R,2R,3R)-1-methoxycarbonyl-trans-2-(4-bromophenyl)-cis-3-[(E)-2-(trimethylsilyl)vinyl]cyclopropane(1160615-46-2)
EPA Substance Registry System: (1R,2R,3R)-1-methoxycarbonyl-trans-2-(4-bromophenyl)-cis-3-[(E)-2-(trimethylsilyl)vinyl]cyclopropane(1160615-46-2)

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: 1160615-46-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1160615-46-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,0,6,1 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1160615-46:
(9*1)+(8*1)+(7*6)+(6*0)+(5*6)+(4*1)+(3*5)+(2*4)+(1*6)=122
122 % 10 = 2
So 1160615-46-2 is a valid CAS Registry Number.

1160615-46-2Upstream product

3650-78-0 methyl 4-bromocinnamate

1160615-46-2Downstream Products

1160615-46-2Relevant academic research and scientific papers

First example of highly stereoselective synthesis of 1,2,3-trisubstituted cyclopropanes via chiral selenonium ylides

Wang, Hai-Yang,Yang, Fei,Li, Xin-Liang,Yan, Xue-Ming,Huang, Zhi-Zhen

supporting information; experimental part, p. 3784 - 3789 (2009/12/07)

As the first example of the application of chiral selenonium ylides in asymmetric cyclopropanation, a new strategy for the highly stereoselective synthesis of chiral 1,2,3-trisubstituted cyclopropanes via selenonium ylides is described. The reaction affor

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