Cas 149495-88-5,Acetic acid (S)-2,2,2-trifluoro-1-(5-trimethylsilanyl-furan-2-yl)-ethyl ester

149495-88-5

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Basic information

Product Name: Acetic acid (S)-2,2,2-trifluoro-1-(5-trimethylsilanyl-furan-2-yl)-ethyl ester
Synonyms: Acetic acid (S)-2,2,2-trifluoro-1-(5-trimethylsilanyl-furan-2-yl)-ethyl ester
CAS NO:149495-88-5
Molecular Formula:
Molecular Weight: 280.319
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: Acetic acid (S)-2,2,2-trifluoro-1-(5-trimethylsilanyl-furan-2-yl)-ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid (S)-2,2,2-trifluoro-1-(5-trimethylsilanyl-furan-2-yl)-ethyl ester(149495-88-5)
EPA Substance Registry System: Acetic acid (S)-2,2,2-trifluoro-1-(5-trimethylsilanyl-furan-2-yl)-ethyl ester(149495-88-5)

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: 149495-88-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 149495-88-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,4,9 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 149495-88:
(8*1)+(7*4)+(6*9)+(5*4)+(4*9)+(3*5)+(2*8)+(1*8)=185
185 % 10 = 5
So 149495-88-5 is a valid CAS Registry Number.

149495-88-5Upstream product

1578-33-2 2-furyltrimethylsilane

149495-88-5Downstream Products

149495-88-5Relevant 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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