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7-METHYL-7-OCTEN-5-YN-3-OL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87371-34-4

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87371-34-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87371-34-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,3,7 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 87371-34:
(7*8)+(6*7)+(5*3)+(4*7)+(3*1)+(2*3)+(1*4)=154
154 % 10 = 4
So 87371-34-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H14O/c1-4-9(10)7-5-6-8(2)3/h9-10H,2,4,7H2,1,3H3/t9-/m1/s1

87371-34-4SDS

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 7-methyloct-7-en-5-yn-3-ol

1.2 Other means of identification

Product number -
Other names 7-METHYL-7-OCTEN-5-YN-3-OL

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:87371-34-4 SDS

87371-34-4Downstream Products

87371-34-4Relevant academic research and scientific papers

A new method for the synthesis of Z-enediones via IBX-mediated oxidative rearrangement of 2-alkynyl alcohol systems

Crone, Benedikt,Kirsch, Stefan F.

, p. 764 - 766 (2006)

o-Iodoxybenzoic acid (IBX) was found to mediate the conversion of α-alkynyl alcohols into Z-enediones under notably mild conditions via a novel rearrangement mechanism (33-65% yield, 13 examples). The Royal Society of Chemistry 2006.

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