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39872-54-3

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39872-54-3 Usage

Chemical structure

A cyclopentadiene ring with a methoxymethyl group attached to one of its carbon atoms.

Physical state

Colorless liquid.

Molecular weight

122.16 g/mol.

Uses

Building block in the synthesis of various organic compounds and pharmaceutical products; used in the production of polymers and other specialty chemicals.

Functionality

Methoxymethyl group provides stability to the cyclopentadiene ring and allows for various functionalization reactions.

Versatility

Acts as a versatile intermediate in organic synthesis.

Safety precautions

Handle with caution due to potential health and safety risks.

Check Digit Verification of cas no

The CAS Registry Mumber 39872-54-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,8,7 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 39872-54:
(7*3)+(6*9)+(5*8)+(4*7)+(3*2)+(2*5)+(1*4)=163
163 % 10 = 3
So 39872-54-3 is a valid CAS Registry Number.

39872-54-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(methoxymethyl)cyclopenta-1,3-diene

1.2 Other means of identification

Product number -
Other names 5-methoxymethyl-cyclopenta-1,3-diene

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:39872-54-3 SDS

39872-54-3Relevant articles and documents

CYCLIC UNSATURATED COMPOUNDS. LXXII. ALKOXYCYCLOPENTADIENES

Mironov, V. A.,Luk'yanov, V. T.,Bernadskii, A. A.

, p. 61 - 70 (2007/10/02)

A convenient method was developed for the synthesis of alkoxycyclopentadienes from the relatively easily obtainable 3-hydroxytricyclo2,6>deca-4,8-diene.It was shown that the obtained substances are equilibrium mixtures of isomers with respect to the position of the system of intracyclic double bonds and contain 1- and 2-substituted cyclopentadienes in a ratio 1:2 respectively.If the alkoxy group is removed from the cyclopentadiene ring, the ratio of the isomers (1:1.5) approximates to that for alkylcyclopentadienes.

Stereospecific total synthesis of prostaglandins E3 and F3 alpha.

Corey,Shirahama,Yamamoto,Terashima,Venkateswarlu,Schaaf

, p. 1490 - 1491 (2007/10/16)

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