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1573-66-6

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1573-66-6 Usage

General Description

1-Hexen-5-yn-3-ol, also known as hex-5-yn-3-ol, is a chemical compound with the molecular formula C6H8O. It is classified as an alcohol and is characterized by the presence of both a double bond and a triple bond in its carbon chain. 1-Hexen-5-yn-3-ol is commonly used in organic synthesis and chemical research and has been studied for its potential applications in the pharmaceutical and fragrance industries. It is a colorless liquid with a distinct odor and is considered to be a moderately hazardous substance, with potential health and environmental risks associated with its use and handling.

Check Digit Verification of cas no

The CAS Registry Mumber 1573-66-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,7 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1573-66:
(6*1)+(5*5)+(4*7)+(3*3)+(2*6)+(1*6)=86
86 % 10 = 6
So 1573-66-6 is a valid CAS Registry Number.

1573-66-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name hex-1-en-5-yn-3-ol

1.2 Other means of identification

Product number -
Other names (+/-)-1-hexen-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:1573-66-6 SDS

1573-66-6Relevant articles and documents

Nonracemic homopropargylic alcohols via asymmetric allenylboration with the robust and versatile 10-TMS-9-borabicyclo[3.3.2]decanes

Lai, Chunqiu,Soderquist, John A.

, p. 799 - 802 (2007/10/03)

(Chemical Equation Presented) The asymmetric allenylboration of representative aldehydes with the stable, storable 1 is reported. Easily and efficiently prepared in either enantiomeric form from the air-stable crystalline 4 through simple Grignard procedures, 1 gives 6 cleanly. The latter is easily isolated in high yield and ee with predictable stereochemistry. The procedure also regenerates 4 for its direct conversion back to 1 and facilitates the efficient recovery of the pseudoephedrine. The net process is the synthetic equivalent of the asymmetric addition of allenylmagnesium bromide to aldehydes.

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