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4495-52-7

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4495-52-7 Usage

Appearance

Colorless liquid

Odor

Strong ammonia-like

Salt form

Dihydrochloride

Uses

a. Corrosion inhibitor
b. Curing agent in epoxy resin formulations
c. Pharmaceutical applications
d. Starting material for organic compound synthesis

Hazardous properties

a. Skin and eye irritation
b. Harmful if ingested
c. Harmful if inhaled

Handling precautions

Handle with care due to hazardous nature

Check Digit Verification of cas no

The CAS Registry Mumber 4495-52-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,9 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4495-52:
(6*4)+(5*4)+(4*9)+(3*5)+(2*5)+(1*2)=107
107 % 10 = 7
So 4495-52-7 is a valid CAS Registry Number.

4495-52-7SDS

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 1,2-ETHANEDIAMINE, N,N''-DICYCLOHEXYL-, DIHYDROCHLORIDE

1.2 Other means of identification

Product number -
Other names N,N'-dicyclohexyl-ethylenediamine,dihydrochloride

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:4495-52-7 SDS

4495-52-7Downstream Products

4495-52-7Relevant articles and documents

Ni-Catalyzed Dual C-H Annulation of Benzimidazoles with Alkynes for Synthesis of π-Extended Heteroarenes

Qi, Shao-Long,Li, Yue,Li, Jiang-Fei,Zhang, Tao,Luan, Yu-Xin,Ye, Mengchun

supporting information, p. 4034 - 4039 (2021/05/26)

Transition metal catalyzed dual C-H activation and annulation with alkynes was an attractive protocol to construct polycyclic π-extended structures. However, most of them were dominated by noble metal catalysts. Disclosed herein was the study of base-metal Ni-catalysis for dual C-H annulation of N-aromatic imidazole, which produced a range of desired polycyclic aza-quinolines in 48-95% yields. The use of bifunctional phosphine oxide ligand proved to be critical for success.

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