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1014-41-1

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1014-41-1 Usage

Physical state

Colorless liquid

Odor

Sweet, floral

Uses

a. Solvent
b. Manufacturing of other chemicals
c. Production of lubricants
d. Production of fuels
e. Production of petrochemicals
f. Intermediate in synthesis of agrochemicals
g. Intermediate in synthesis of pharmaceuticals

Flammability

Flammable

Health hazards

May cause skin irritation upon contact

Environmental impact

Prolonged exposure to high concentrations may have harmful effects on human health and the environment

Safety precautions

Proper handling and disposal required

Check Digit Verification of cas no

The CAS Registry Mumber 1014-41-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,1 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1014-41:
(6*1)+(5*0)+(4*1)+(3*4)+(2*4)+(1*1)=31
31 % 10 = 1
So 1014-41-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H22/c1-5-11(3)13-7-9-14(10-8-13)12(4)6-2/h7-12H,5-6H2,1-4H3

1014-41-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-di(butan-2-yl)benzene

1.2 Other means of identification

Product number -
Other names Benzene,1,4-bis-(1-methylpropyl)

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:1014-41-1 SDS

1014-41-1Relevant articles and documents

-

McKenna,Sowa

, p. 470 (1937)

-

Burwell,Archer

, p. 1032 (1942)

Alkylation of benzene with 1-butene in the presence of AlCl3

Kharlampidi,Izmailov,Batyrshin

, p. 278 - 280 (2007/10/03)

The catalytic alkylation of benzene with 1-butene at 20-50×C and varied amounts of the AlCl3 catalyst was studied with the aim of optimization of the method of synthesis of sec-butylbenzene. By means of NMR and IR spectroscopy it was shown that together with the main product, sec-butylbenzene the reaction gives 1,3- and 1,4-di-sec-butylbenzenes. The alkylation conditions that allow preparation of sec-butylbenzene and its subsequent isomerization to isobutylbenzene were found.

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