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3102-71-4

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3102-71-4 Usage

Chemical compound

Used in organic synthesis and pharmaceutical research

Molecular weight

270.40 g/mol

Physical state

Colorless to pale yellow liquid

Odor

Faint

Solubility

Insoluble in water, soluble in organic solvents

Applications

Building block in the synthesis of various organic compounds, development of pharmaceuticals and agrochemicals

Additional use

Cross-linking agent in the production of polymers and resins

Safety

Potential health hazards and reactivity, requires proper handling and storage procedures

Check Digit Verification of cas no

The CAS Registry Mumber 3102-71-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,0 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3102-71:
(6*3)+(5*1)+(4*0)+(3*2)+(2*7)+(1*1)=44
44 % 10 = 4
So 3102-71-4 is a valid CAS Registry Number.

3102-71-4SDS

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 4,6-di(propan-2-yl)benzene-1,3-diamine

1.2 Other means of identification

Product number -
Other names 1,3-DIAMINO-4,6-DIISOPROPYLBENZENE

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:3102-71-4 SDS

3102-71-4Relevant articles and documents

Synthesis and conformational properties of tetranitroazacalix[4]arenes

Konishi, Hisatoshi,Hashimoto, Shun,Sakakibara, Terunobu,Matsubara, Shingo,Yasukawa, Yusuke,Morikawa, Osamu,Kobayashi, Kazuhiro

, p. 620 - 623 (2009)

Tetranitroazacalix[4]arenes have been synthesized by the nucleophilic aromatic substitution of 1,5-difluoro-2,4-dinitrobenzene with 1,3-diaminobenzenes. An X-ray crystal structure analysis revealed that the azacalixarenes adopt a non-symmetrical 1,3-alter

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