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174064-00-7

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174064-00-7 Usage

General Description

7-TETRADECYN-6,9-DIOL is a chemical compound with the molecular formula C14H24O2. It is a diol, meaning it contains two hydroxyl functional groups. 7-TETRADECYN-6,9-DIOL is a long-chain, linear molecule, with a terminal alkyne group located at the sixth carbon and hydroxyl groups at the sixth and ninth carbons. It is primarily used in organic synthesis as a reactant in the production of various compounds, including pharmaceuticals, agrochemicals, and polymers. This chemical has potential applications in the fields of medicine, agriculture, and materials science due to its unique structure and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 174064-00-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,0,6 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 174064-00:
(8*1)+(7*7)+(6*4)+(5*0)+(4*6)+(3*4)+(2*0)+(1*0)=117
117 % 10 = 7
So 174064-00-7 is a valid CAS Registry Number.

174064-00-7SDS

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 tetradec-7-yne-6,9-diol

1.2 Other means of identification

Product number -
Other names 7-TETRADECYN-6,9-DIOL

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:174064-00-7 SDS

174064-00-7Downstream Products

174064-00-7Relevant articles and documents

[3,3]-Sigmatropic Rearrangements in the Enantioselective Synthesis of (-)-Methylenolactocin

Ariza, Xavier,Fernández, Natalia,Garcia, Jordi,López, Marta,Montserrat, Laia,Ortiz, Jordi

, p. 128 - 134 (2004)

A Pd(II)-catalyzed [3,3]-sigmatropic rearrangement is used to transfer chirality from an enantio-enriched alk-3-ene-1,2-diol to a C2- symmetrical alk-2-ene-1,4-diol which, in turn, can be converted into a precursor of (-)-methylenolactocin through an additional [3,3]-sigmatropic rearrangement (either Johnson orthoester or Ireland-Claisen rearrangement).

Unsaturated syn - And anti -1,2-amino alcohols by cyclization of allylic bis-trichloroacetimidates. Stereoselectivity dependence on substrate configuration

Grigorjeva, Liene,Kinens, Artis,Jirgensons, Aigars

, p. 920 - 927 (2015)

Disubstituted allylic bis-imidates undergo Lewis acid catalyzed or spontaneous cyclization to oxazolines, which are precursors of unsaturated amino alcohols. Stereoselectivity of the cyclization is mainly determined by the substrate configuration. Highly

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