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2(3H)-Furanone, 3-(4-chlorophenyl)dihydro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91154-09-5

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91154-09-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91154-09-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,1,5 and 4 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 91154-09:
(7*9)+(6*1)+(5*1)+(4*5)+(3*4)+(2*0)+(1*9)=115
115 % 10 = 5
So 91154-09-5 is a valid CAS Registry Number.

91154-09-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-chlorophenyl)oxolan-2-one

1.2 Other means of identification

Product number -
Other names 3-(4-chlorophenyl)dihydrofuran-2(3H)-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:91154-09-5 SDS

91154-09-5Relevant academic research and scientific papers

Weak arene C-h×××o hydrogen bonding in palladium-catalyzed arylation and vinylation of lactones

Huang, Zhiyan,Chen, Zuliang,Lim, Li Hui,Quang, Gia Chuong Phan,Hirao, Hajime,Zhou, Jianrong

supporting information, p. 5807 - 5812 (2013/07/05)

Weak force in action: In the title reaction, the palladium catalyst (see figure, left) uses weak CH×××O hydrogen bonding to control the absolute configuration of the new stereocenter. A similar palladium catalyst (right) used conventional NH×××O hydrogen bonding to guide stereoselection. Copyright

Enantioselective acylation of silyl ketene acetals through fluoride anion-binding catalysis

Birrell, James A.,Desrosiers, Jean-Nicolas,Jacobsen, Eric N.

supporting information; experimental part, p. 13872 - 13875 (2011/10/09)

A highly enantioselective acylation of silyl ketene acetals with acyl fluorides has been developed to generate useful α,α-disubstituted butyrolactone products. This transformation is promoted by a new thiourea catalyst and 4-pyrrolidinopyridine and represents the first example of enantioselective thiourea anion-binding catalysis with fluoride.

GEMINALLY SUBSTITUTED CYCLIC ETHER CARBOXYLIC ACIDS, DERIVATIVES, THEREOF, COMOPOSITIONS CONTAINING SAME AND METHOD OF USE

-

, (2008/06/13)

Geminally-substituted cyclic ether carboxylic acids or derivatives thereof are provided which have the structure STR1 wherein Z is aryl, which may be optionally substituted with one or more of the following groups: halo, lower alkyl, lower alkoxy, hydroxy, lower alkylamino, phenyl or carbo-lower alkoxy STR2 R is COOH, COO alkali metal, coo lower alkyl, STR3 R 1 is lower alkyl or aryl; n is 1 or 2;p is 2 to 5; andq is 1 to 4.These compounds are cardiovascular agents which exhibit thromboxane antagonist activity and thus are useful in the treatment of thrombotic disease.

A NEW SYNTHESIS OF trans-2-SUBSTITUTED-2-BUTENE-1,4-DIOLS FROM 2-BUTYNE-1,4-DIOL VIA NUCLEOPHILIC ADDITION OF GRIGNARD REAGENTS

Ishino, Yoshio,Wakamoto, Kohji,Hirashima, Tsuneaki

, p. 765 - 768 (2007/10/02)

trans-2-Substituted-2-butene-1,4-diols were readily obtained by reactions of 2-butyne-1,4-diol with Grignard reagents in good yields.

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