Cas 140404-40-6,2-[(S)-1-(tert-Butyl-dimethyl-silanyloxy)-2,2,2-trifluoro-ethyl]-5-trimethylsilanyl-furan

140404-40-6

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Basic information

Product Name: 2-[(S)-1-(tert-Butyl-dimethyl-silanyloxy)-2,2,2-trifluoro-ethyl]-5-trimethylsilanyl-furan
Synonyms: 2-[(S)-1-(tert-Butyl-dimethyl-silanyloxy)-2,2,2-trifluoro-ethyl]-5-trimethylsilanyl-furan
CAS NO:140404-40-6
Molecular Formula:
Molecular Weight: 352.544
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: 2-[(S)-1-(tert-Butyl-dimethyl-silanyloxy)-2,2,2-trifluoro-ethyl]-5-trimethylsilanyl-furan(CAS DataBase Reference)
NIST Chemistry Reference: 2-[(S)-1-(tert-Butyl-dimethyl-silanyloxy)-2,2,2-trifluoro-ethyl]-5-trimethylsilanyl-furan(140404-40-6)
EPA Substance Registry System: 2-[(S)-1-(tert-Butyl-dimethyl-silanyloxy)-2,2,2-trifluoro-ethyl]-5-trimethylsilanyl-furan(140404-40-6)

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: 140404-40-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 140404-40-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,4,0 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 140404-40:
(8*1)+(7*4)+(6*0)+(5*4)+(4*0)+(3*4)+(2*4)+(1*0)=76
76 % 10 = 6
So 140404-40-6 is a valid CAS Registry Number.

140404-40-6Upstream product

1578-33-2 2-furyltrimethylsilane

140404-40-6Downstream Products

140404-40-6Relevant academic research and scientific papers

Chiral Trifluoromethylated 2-Butenolides for the Construction of 6-Deoxy-6,6,6-trifluorosugars

Yamazaki, Takashi,Mizutani, Kenji,Takeda, Mitsunori,Kitazume, Tomoya

, p. 55 - 57 (2007/10/02)

Optically active 2-butenolides with a trifluoromethyl (CF3) group are synthesized via enzymatic optical resolution and are selectively transformed into 6,6,6-trifluororhodinose and amicetose by base-promoted 1,2-migration of a tert-butyldimethylsilyl moiety in a highly efficient manner.

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