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88274-91-3

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88274-91-3 Usage

Unsaturated alcohol

Alkynol
Contains both a triple bond and a hydroxyl group in its chemical structure.

Classification

Fatty alcohol
Commonly found in biological membranes and lipid structures.

Usage

Building block in synthetic and organic chemistry
Used for the synthesis of various compounds.

(E)designation

Trans-configuration
Indicates that the double bond in the compound has the two highest priority groups on opposite sides.

Check Digit Verification of cas no

The CAS Registry Mumber 88274-91-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,2,7 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 88274-91:
(7*8)+(6*8)+(5*2)+(4*7)+(3*4)+(2*9)+(1*1)=173
173 % 10 = 3
So 88274-91-3 is a valid CAS Registry Number.

88274-91-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-13-hexadecen-11-yn-1-ol

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:88274-91-3 SDS

88274-91-3Downstream Products

88274-91-3Relevant articles and documents

A STEREOSELECTIVE SYNTHESIS OF (Z)-13-HEXADECEN-11-YNYL ACETATE, THE SEX PHEROMONE OF Thaumetopoea pityocampa (LEPIDOPTERA, NOTODONTIDAE)

Cardillo, Giuliana,Cugola, Alfredo,Orena, Mario,Sandri, Sergio

, p. 231 - 234 (2007/10/02)

(Z)-13-Hexadecen-11-ynyl acetate, 1, the sex pheromone of Thaumetopoea pityocampa, has been synthesized stereospecifically, starting from anion of 3--1-hexyne, 8, which was alkylated with 10-iodo-1-decane; the intermediate diol 2, obtained upon removal of the protecting groups was stereoselectively dehydrated with KHSO4.

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