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Heptadecane, 7-methylene- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51655-67-5

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51655-67-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51655-67-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,6,5 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 51655-67:
(7*5)+(6*1)+(5*6)+(4*5)+(3*5)+(2*6)+(1*7)=125
125 % 10 = 5
So 51655-67-5 is a valid CAS Registry Number.

51655-67-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-methylideneheptadecane

1.2 Other means of identification

Product number -
Other names Heptadecane,7-methylene

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:51655-67-5 SDS

51655-67-5Downstream Products

51655-67-5Relevant academic research and scientific papers

Alkylzirconation of alkynes catalyzed by triphenylcarbenium tetrakis(pentafluorophenyl)borate

Yamanoi, Shigeo,Ohrui, Hiroki,Seki, Kentaro,Matsumoto, Takashi,Suzuki, Keisuke

, p. 8407 - 8410 (2007/10/03)

[(C6H5)3C]+[B(C6F5)4]- effectively catalyzes the alkylmetallation of alkynes by using the alkylzirconium species, which is generated by the hydrozirconation of alkenes

Cobalt-catalyzed alkenylation of organomagnesium reagents

Cahiez, Gerard,Avedissian, Hovsep

, p. 6159 - 6162 (2007/10/03)

Alkenyl iodides, bromides and chlorides react with organomagnesium reagents in THF, in the presence of Co(acac)2 and NMP (9 to 4 equiv.), to give the cross-coupling products in good yields. The reaction is chemoselective (aryl or alkyl bromides, esters and ketones) and stereoselective (≤ 99.5%).

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