Cas 1151770-69-2,(1S,2S)-methyl 1-(4-bromophenyl)-2-(tert-butyldimethylsilyloxy)-2-(4-(trifluoromethyl)phenyl)cyclopropanecarboxylate

1151770-69-2

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Basic information

Product Name: (1S,2S)-methyl 1-(4-bromophenyl)-2-(tert-butyldimethylsilyloxy)-2-(4-(trifluoromethyl)phenyl)cyclopropanecarboxylate
Synonyms:
CAS NO:1151770-69-2
Molecular Formula:
Molecular Weight: 529.469
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: (1S,2S)-methyl 1-(4-bromophenyl)-2-(tert-butyldimethylsilyloxy)-2-(4-(trifluoromethyl)phenyl)cyclopropanecarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (1S,2S)-methyl 1-(4-bromophenyl)-2-(tert-butyldimethylsilyloxy)-2-(4-(trifluoromethyl)phenyl)cyclopropanecarboxylate(1151770-69-2)
EPA Substance Registry System: (1S,2S)-methyl 1-(4-bromophenyl)-2-(tert-butyldimethylsilyloxy)-2-(4-(trifluoromethyl)phenyl)cyclopropanecarboxylate(1151770-69-2)

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: 1151770-69-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1151770-69-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,1,7,7 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1151770-69:
(9*1)+(8*1)+(7*5)+(6*1)+(5*7)+(4*7)+(3*0)+(2*6)+(1*9)=142
142 % 10 = 2
So 1151770-69-2 is a valid CAS Registry Number.

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1151770-69-2Relevant academic research and scientific papers

Intermolecular C-H functionalization versus cyclopropanation of electron rich 1,1-disubstituted and trisubstituted alkenes

Ventura, Dominic L.,Li, Zhanjie,Coleman, Michael G.,Davies, Huw M.L.

supporting information; experimental part, p. 3052 - 3061 (2009/09/06)

Rhodium(II)-catalyzed reactions of aryldiazoacetates with electron rich 1,1-disubstituted and trisubstituted alkenes were systematically studied. The regio-, diastereo- and enantioselectivity of the chemistry was profoundly influenced by the nature of the

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