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135511-17-0

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135511-17-0 Usage

General Description

HEPT-4-EN-6-YN-1-OL is a chemical compound with the molecular formula C7H10O. It is an unsaturated alcohol containing a heptene chain with a triple bond at the sixth position and a hydroxyl group at the first position. HEPT-4-EN-6-YN-1-OL is commonly used in organic synthesis as a building block for creating various molecules and pharmaceuticals. It has a yellowish color and a mild odor, and it is flammable in nature. Proper handling and storage of HEPT-4-EN-6-YN-1-OL are required to ensure safety and prevent any potential hazards associated with its use.

Check Digit Verification of cas no

The CAS Registry Mumber 135511-17-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,5,1 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 135511-17:
(8*1)+(7*3)+(6*5)+(5*5)+(4*1)+(3*1)+(2*1)+(1*7)=100
100 % 10 = 0
So 135511-17-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H10O/c1-2-3-4-5-6-7-8/h1,3-4,8H,5-7H2/b4-3+

135511-17-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name HEPT-4-EN-6-YN-1-OL

1.2 Other means of identification

Product number -
Other names 4-Hepten-6-yn-1-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:135511-17-0 SDS

135511-17-0Relevant articles and documents

A novel synthesis of trans-enynes from substituted tetrahydropyrans

Karadogan, Burhan,Edwards, Neil,Parsons, Philip J.

, p. 5931 - 5934 (1999)

A novel method for the synthesis of trans-enynes is described, which relies on a butyllithium induced ring scission of 3-bromo-2- ethynyltetrahydropyrans.

Butyllithium-induced dimerization of pent-3-en-1-yne and related additions

Klusener, P. A. A.,Hommes, H.,Hanekamp, J. C.,Kerk, A. C. H. T. M. van der,Brandsma, L.

, p. 67 - 81 (2007/10/02)

The enynes HCCCH=CHCH2R (R = H, Me, OMe, NMe2, SMe), are converted into dimers by treatment with slightly more than two equivalents of butyllithium.The Z-configuration predominates in the dimers obtained after aqueous work-up.The lithiated enynes (R = H, Me, SMe) and acetylenic compounds LiCCCH2R (R = SMe, C6H5) add in an analogous way to the double bond of LiCCCH=CH2.

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