Cas 876156-54-6,(2R,3S)-METHYL 2-(2-FLUOROPHENYL)-3-(TRIFLUOROMETHYL)-1,4-OXATHIANE-3-CARBOXYLATE

876156-54-6

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Basic information

Product Name: (2R,3S)-METHYL 2-(2-FLUOROPHENYL)-3-(TRIFLUOROMETHYL)-1,4-OXATHIANE-3-CARBOXYLATE
Synonyms: (2R,3S)-METHYL 2-(2-FLUOROPHENYL)-3-(TRIFLUOROMETHYL)-1,4-OXATHIANE-3-CARBOXYLATE
CAS NO:876156-54-6
Molecular Formula: C13H12F4O3S
Molecular Weight: 0
EINECS: N/A
Product Categories: N/A
Mol File: 876156-54-6.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (2R,3S)-METHYL 2-(2-FLUOROPHENYL)-3-(TRIFLUOROMETHYL)-1,4-OXATHIANE-3-CARBOXYLATE(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3S)-METHYL 2-(2-FLUOROPHENYL)-3-(TRIFLUOROMETHYL)-1,4-OXATHIANE-3-CARBOXYLATE(876156-54-6)
EPA Substance Registry System: (2R,3S)-METHYL 2-(2-FLUOROPHENYL)-3-(TRIFLUOROMETHYL)-1,4-OXATHIANE-3-CARBOXYLATE(876156-54-6)

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: 876156-54-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 876156-54-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,6,1,5 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 876156-54:
(8*8)+(7*7)+(6*6)+(5*1)+(4*5)+(3*6)+(2*5)+(1*4)=206
206 % 10 = 6
So 876156-54-6 is a valid CAS Registry Number.

876156-54-6Upstream product

173558-71-9 2-diazo-3,3,3-trifluoropropionic acid methyl ester

876156-54-6Downstream Products

876156-54-6Relevant articles and documents

Stereoselective preparation of trifluoromethyl containing 1,4-oxathiolane derivatives through ring expansion reaction of 1,3-oxathiolanes

Zhu, Shifa,Xing, Chunhui,Zhu, Shizheng

, p. 829 - 832 (2007/10/03)

Trifluoromethyl containing 1,4-oxathiolanes are synthesized in excellent yields and high stereoselectivities from the expansion reactions of sulfur ylide intermediates, which were prepared from the reaction of 2-diazo-3,3,3- trifluoro-propionic acid methy

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