Cas 178232-48-9,(S)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (1R,2S)-2-[1-((R)-toluene-4-sulfinylmethyl)-vinyloxy]-cyclopentyl ester

178232-48-9

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Basic information

Product Name: (S)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (1R,2S)-2-[1-((R)-toluene-4-sulfinylmethyl)-vinyloxy]-cyclopentyl ester
Synonyms: (S)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (1R,2S)-2-[1-((R)-toluene-4-sulfinylmethyl)-vinyloxy]-cyclopentyl ester
CAS NO:178232-48-9
Molecular Formula:
Molecular Weight: 496.548
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: (S)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (1R,2S)-2-[1-((R)-toluene-4-sulfinylmethyl)-vinyloxy]-cyclopentyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (1R,2S)-2-[1-((R)-toluene-4-sulfinylmethyl)-vinyloxy]-cyclopentyl ester(178232-48-9)
EPA Substance Registry System: (S)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (1R,2S)-2-[1-((R)-toluene-4-sulfinylmethyl)-vinyloxy]-cyclopentyl ester(178232-48-9)

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: 178232-48-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 178232-48-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,8,2,3 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 178232-48:
(8*1)+(7*7)+(6*8)+(5*2)+(4*3)+(3*2)+(2*4)+(1*8)=149
149 % 10 = 9
So 178232-48-9 is a valid CAS Registry Number.

178232-48-9Upstream product

178232-48-9Downstream Products

178232-48-9Relevant academic research and scientific papers

Novel asymmetric desymmetrization of meso-1,2-diols via diastereoselective β-elimination of chiral α-arylsulfinyl acetals

Maezaki, Naoyoshi,Soejima, Motohiro,Takeda, Miwako,Sakamoto, Atsunobu,Matsumori, Yuki,Tanaka, Tetsuaki,Iwata, Chuzo

, p. 6527 - 6546 (2007/10/03)

Enantioselective desymmetrization of meso-1,2-diols was accomplished via diastereoselective C-O bond fission of acetals derived from various optically active β-ketosulfoxides with high diastereoselectivities. The substituent at the γ-position of the β-ketosulfoxide plays an important role in this cleavage.

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