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Benzene, 1-chloro-4-(3-methyl-1-butenyl)-, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89130-31-4

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89130-31-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89130-31-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,1,3 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 89130-31:
(7*8)+(6*9)+(5*1)+(4*3)+(3*0)+(2*3)+(1*1)=134
134 % 10 = 4
So 89130-31-4 is a valid CAS Registry Number.

89130-31-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Chloro-4-((Z)-3-methyl-but-1-enyl)-benzene

1.2 Other means of identification

Product number -
Other names -

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:89130-31-4 SDS

89130-31-4Downstream Products

89130-31-4Relevant academic research and scientific papers

Visible-light-mediated alkylation of 4-alkyl-1,4-dihydropyridines with alkenyl sulfones

Dong, Jianyang,Liu, Yuxiu,Wang, Qingmin,Yue, Fuyang

, p. 8924 - 8928 (2021/11/04)

Herein we report a mild, general protocol for visible-light-mediated alkylation of 4-alkyl-1,4-dihydropyridines with alkenyl sulfones. The protocol permits efficient functionalization of sulfones with a broad range of cyclic and acyclic secondary and tert

OLEFIN SYNTHESIS USING LITHIUM DERIVATIVES OF N,N,N',N'-TETRAMETHYLDIAMIDES OF ARYLMETHANEPHOSPHONIC ACIDS

Petrova, Jordanka,Kirilov, Marko,Momchilova, Snejana

, p. 29 - 36 (2007/10/02)

The reaction of lithium derivatives of N,N,N',N'-tetramethyldiamides of arylmethanephophonic acids (1-Li) with aldehydes 2 is studied.It is found that under certain reaction conditions (THF, 5 hrs at -70 deg C and then allowing to warm to room temperature) the aldol stage of the reaction is highly stereoselective, only erythro adducts (2-hydroxyphosphonamides) 3, 4 being formed in 47-75percent yields.By heating of 3 and 4 in neutral medium the corresponding (Z)-olefins 5, 6 are obtained (yields 64-74percent).It is established that an acid catalyzed olefination of 2-hydroxyphosphonamides is also possible, but the reaction is not stereospecific.

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