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1160-74-3

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1160-74-3 Usage

General Description

1-[1-[2-(2,4-Dinitrophenyl)hydrazono]ethyl]cyclohexane is a chemical compound with a complex structure. It contains a cyclohexane ring with a hydrazone group attached to it, which in turn is connected to a 2,4-dinitrophenyl group. The presence of a hydrazone group suggests that the compound may have potential applications in organic chemistry as a reagent for the formation of other organic compounds. The 2,4-dinitrophenyl group indicates that the compound may have some potential as a dye or colorant. Additionally, the presence of a cyclohexane ring suggests that the compound may have some applications in the field of materials science or as a precursor for the synthesis of other cyclohexane derivatives. Overall, this compound has the potential for a variety of chemical and material applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1160-74-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,6 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1160-74:
(6*1)+(5*1)+(4*6)+(3*0)+(2*7)+(1*4)=53
53 % 10 = 3
So 1160-74-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H18N4O4/c1-10(11-5-3-2-4-6-11)15-16-13-8-7-12(17(19)20)9-14(13)18(21)22/h7-9,11,16H,2-6H2,1H3

1160-74-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(1-cyclohexylethylideneamino)-2,4-dinitroaniline

1.2 Other means of identification

Product number -
Other names 2,4-Dinitrophenylhydrazon v. Cyclohexyl-methyl-keton

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:1160-74-3 SDS

1160-74-3Relevant articles and documents

New Methods and Reagents in Organic Synthesis; 73. Trimethylsilyldiazomethane: A Convenient Reagent for the Conversion of Aliphatic Aldehydes to the Homologous Methyl Ketones

Aoyama, Toyohiko,Shioiri, Takayuki

, p. 228 - 229 (2007/10/02)

Trimethylsilyldiazomethane reacts smoothly with aliphatic aldehydes in the presence of magnesium bromide (1.5 eqiv) to give homologous methyl ketones after direct treatment with 10percent hydrochloric acid/methanol (1:1).

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