Cas 1187549-75-2,(S)-4-fluoro-3-phenylbutan-1-ol

1187549-75-2

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Basic information

Product Name: (S)-4-fluoro-3-phenylbutan-1-ol
Synonyms: (S)-4-fluoro-3-phenylbutan-1-ol
CAS NO:1187549-75-2
Molecular Formula:
Molecular Weight: 168.211
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)-4-fluoro-3-phenylbutan-1-ol(CAS DataBase Reference)
NIST Chemistry Reference: (S)-4-fluoro-3-phenylbutan-1-ol(1187549-75-2)
EPA Substance Registry System: (S)-4-fluoro-3-phenylbutan-1-ol(1187549-75-2)

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: 1187549-75-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1187549-75-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,7,5,4 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1187549-75:
(9*1)+(8*1)+(7*8)+(6*7)+(5*5)+(4*4)+(3*9)+(2*7)+(1*5)=202
202 % 10 = 2
So 1187549-75-2 is a valid CAS Registry Number.

1187549-75-2Upstream product

1187549-75-2Downstream Products

1187549-78-5 (S)-4-fluoro-3-phenylbutanal

1187549-75-2Relevant academic research and scientific papers

1,3-Benzodithiole-1,1,3,3-tetraoxide (BDT) as a versatile methylation reagent in catalytic enantioselective Michael addition reaction with enals

Zhang, Shilei,Li, Jian,Zhao, Sihan,Wang, Wei

supporting information; experimental part, p. 1766 - 1769 (2010/05/19)

A protocol of an organocatalytic highly enantioselective conjugate addition of nucleophilic BDT to enals has been developed and the versatile Michael adducts serve as useful building blocks for a variety of organic transformations.

Formal highly enantioselective organocatalytic addition of fluoromethyl anion to α,β-unsaturated aldehydes

Alba, Andrea-Nekane,Companyo, Xavier,Moyano, Albert,Rios, Ramon

supporting information; experimental part, p. 7035 - 7038 (2010/03/25)

The first organocatalytic enantioselective fluoro(bis-phenlsulfonyl) methylation of α-β-unsaturated aldehydes in high yields and enantioselective fluoro(bis-phenylsulfonyl) methylation of α-β- unsaturated aldehydes in high yields and enantioselectivity wa

Catalytic enantioselective conjugate addition of fluorobis(phenylsulfonyl) methane to enals: Synthesis of chiral monofluoromethyl compounds

Zhang, Shilei,Zhang, Yinan,Ji, Yafei,Li, Hao,Wang, Wei

supporting information; experimental part, p. 4886 - 4888 (2009/12/08)

A new highly catalytic enantioselective Michael addition of fluorobis(phenylsulfonyl)methane to α,β-unsaturated aldehydes has been developed for the preparation of chiral monofluoromethyl compounds under mild reaction conditions.

Enantioselective organocatalytic conjugate addition of fluorocarbon nucleophiles to α,β-unsaturated aldehydes

Ullah, Farman,Zhao, Gui-Ling,Deiana, Luca,Zhu, Mingzhao,Dziedzic, Pawel,Ibrahem, Ismail,Hammar, Peter,Sun, Junliang,Cordova, Armando

supporting information; experimental part, p. 10013 - 10017 (2010/04/05)

Highly chemo- and enantioselective organocatalytic conjugate additions of fluorocarbon nucleophiles to a,b-unsaturated aldehydes and the construction of a quaternary carbon stereocenter bearing a fluorine atom with high enantioselectivity was reported. Af

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