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138434-36-3

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138434-36-3 Usage

Physical state

Colorless liquid

Odor

Strong

Common uses

a. Solvent
b. Intermediate in the synthesis of other chemicals

Flammability

Highly flammable

Safety precautions

Handle with care

Reactivity

Used as a reagent in organic chemistry reactions

Specific applications

a. Synthesis of aromatic compounds
b. Production of fragrances
c. Production of flavors
d. Production of pharmaceuticals

Check Digit Verification of cas no

The CAS Registry Mumber 138434-36-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,4,3 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 138434-36:
(8*1)+(7*3)+(6*8)+(5*4)+(4*3)+(3*4)+(2*3)+(1*6)=133
133 % 10 = 3
So 138434-36-3 is a valid CAS Registry Number.

138434-36-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-dimethyl-5-propan-2-ylidenecyclohexa-1,3-diene

1.2 Other means of identification

Product number -
Other names 1,3-Cyclohexadiene,2,6-dimethyl-5-(1-methylethylidene)

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:138434-36-3 SDS

138434-36-3Downstream Products

138434-36-3Relevant articles and documents

A Facile Synthesis of 5-Methylene-1,3-cyclohexadienes (o-Isotoluenes) and 1,2,4,6-Heptatetraenes

Andemichael, Yemane W.,Wang, Kung K.

, p. 796 - 798 (2007/10/02)

Condensation between 4-methyl-2,3-pentadienal and γ-(trimethylsilyl)allylboranes 3,4, and 16 followed by Peterson olefination reaction afforded the corresponding o-isotoluenes and diene-allenes.

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