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42981-76-0

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42981-76-0 Usage

Classification

Saturated hydrocarbon, bicyclic aromatic compound

Primary Use

Solvent in industrial applications

Industrial Applications

Production of synthetic resins
Rubber manufacturing
Dye and pigment production

Chemical Intermediate for

Pharmaceuticals synthesis
Agrochemicals synthesis

Physical Properties

Colorless liquid
Mild aromatic odor

Toxicity

Low acute toxicity
High concentrations may cause:
Respiratory system irritation
Skin irritation

Check Digit Verification of cas no

The CAS Registry Mumber 42981-76-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,9,8 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 42981-76:
(7*4)+(6*2)+(5*9)+(4*8)+(3*1)+(2*7)+(1*6)=140
140 % 10 = 0
So 42981-76-0 is a valid CAS Registry Number.
InChI:InChI=1/C18H28/c1-17(2,3)15-9-7-14-12-16(18(4,5)6)10-8-13(14)11-15/h7,9,11,16H,8,10,12H2,1-6H3

42981-76-0SDS

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 2,6-di-t-butyl-1,2,3,4-tetrahydronaphthalene

1.2 Other means of identification

Product number -
Other names 2,6-Di-tert-butyl-1,2,3,4-tetrahydro-naphthalene

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:42981-76-0 SDS

42981-76-0Downstream Products

42981-76-0Relevant articles and documents

Influence of Ring Size on Geminal Interproton Coupling Constants in Exocyclic Methylene Groups

Spear, Robert J.,Sternhell, Sever

, p. 889 - 897 (2007/10/02)

In systems where substituent effects are constant, there is a well defined trend in the magnitude of geminal interproton coupling constants in exocyclic methylene groups with ring size.Reduction of ring size from six to five to four results in a monotonic reduction in the magnitude of Jgem.These trends apply to methylenecycloalkanes, methylenebenzocycloalkenes and α-methylenecycloalkanones.There is an indication that the trend does not continue for methylenecyclopropanes.A number of new exocyclic-methylene compounds have been designed and synthesized to provide specific experimental data.

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