Cas 1436418-79-9,((1S,2R,3S)-2-fluoro-3-(4-(trifluoromethyl)phenyl)cyclopropyl)methanol

1436418-79-9

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Basic information

Product Name: ((1S,2R,3S)-2-fluoro-3-(4-(trifluoromethyl)phenyl)cyclopropyl)methanol
Synonyms: ((1S,2R,3S)-2-fluoro-3-(4-(trifluoromethyl)phenyl)cyclopropyl)methanol
CAS NO:1436418-79-9
Molecular Formula:
Molecular Weight: 234.193
EINECS: N/A
Product Categories: N/A
Mol File: 1436418-79-9.mol
Article Data: 1

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,2R,3S)-2-fluoro-3-(4-(trifluoromethyl)phenyl)cyclopropyl)methanol(CAS DataBase Reference)
NIST Chemistry Reference: ((1S,2R,3S)-2-fluoro-3-(4-(trifluoromethyl)phenyl)cyclopropyl)methanol(1436418-79-9)
EPA Substance Registry System: ((1S,2R,3S)-2-fluoro-3-(4-(trifluoromethyl)phenyl)cyclopropyl)methanol(1436418-79-9)

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: 1436418-79-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1436418-79-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,6,4,1 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1436418-79:
(9*1)+(8*4)+(7*3)+(6*6)+(5*4)+(4*1)+(3*8)+(2*7)+(1*9)=169
169 % 10 = 9
So 1436418-79-9 is a valid CAS Registry Number.

1436418-79-9Upstream product

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1436418-79-9Relevant articles and documents

Highly enantioselective simmons-smith fluorocyclopropanation of allylic alcohols via the halogen scrambling strategy of zinc carbenoids

Beaulieu, Louis-Philippe B.,Schneider, Jakob F.,Charette, Andre B.

supporting information, p. 7819 - 7822 (2013/06/27)

Highly enantio- and diastereoenriched monofluorocyclopropanes were accessed via the Simmons-Smith fluorocyclopropanation of allylic alcohols using difluoroiodomethane and ethylzinc iodide as the substituted carbenoid precursors. The scrambling of halogens

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