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2-Cyclohexyl-1,1,3,3-tetramethylguanidine, also known as Guanidine hydrochloride or Guanidine carbonate, is an organic compound with the chemical formula C9H20N4. It is a derivative of guanidine, a heterocyclic amine, and is characterized by the presence of a cyclohexyl group and two methyl groups attached to the nitrogen atoms. 2-Cyclohexyl-1,1,3,3-tetramethylguanidine is widely used in various applications, including as a catalyst in the synthesis of pharmaceuticals, as a corrosion inhibitor in industrial processes, and as a biocide in water treatment systems. Due to its versatile properties, 2-Cyclohexyl-1,1,3,3-tetramethylguanidine plays a significant role in the chemical industry, contributing to the development of various products and processes.

5012-76-0

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5012-76-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5012-76-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,1 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5012-76:
(6*5)+(5*0)+(4*1)+(3*2)+(2*7)+(1*6)=60
60 % 10 = 0
So 5012-76-0 is a valid CAS Registry Number.

5012-76-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-cyclohexyl-1,1,3,3-tetramethylguanidine

1.2 Other means of identification

Product number -
Other names N''-cyclohexyl-N,N,N',N'-tetramethyl-guanidine

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:5012-76-0 SDS

5012-76-0Downstream Products

5012-76-0Relevant academic research and scientific papers

Synthesis of 3-substituted-4(3H)-quinazolinones via HATU-mediated coupling of 4-hydroxyquinazolines with amines

Xiao, Zili,Yang, Michael G.,Li, Peng,Carter, Percy H.

supporting information; experimental part, p. 1421 - 1424 (2009/09/05)

A novel synthesis of 3-substituted 4(3H)-quinazolinones via HATU-mediated coupling of 4-hydroxyquinazolines with primary amines has been developed. Under mild reaction conditions, the products were achieved in good yield from commercially available starti

Convenient synthesis of oxazolidinones and oxazinones from allyl and homoallyl amines under mild conditions

Garcia-Egido, Eduardo,Fernandez, Isabelle,Munoz, Luis

, p. 3029 - 3042 (2007/10/03)

An efficient one-pot general method for the high-yield synthesis in solution of oxazolidinones and oxazinones from allyl- and homoallylamines, respectively, has been developed. The reaction is carried out at an atmospheric pressure between 0°C and room te

Superbase catalysis of oxazolidin-2-one ring formation from carbon dioxide and prop-2-yn-1-amines under homogeneous or heterogenous conditions

Costa, Mirco,Chiusoli, Gian Paolo,Taffurelli, Davide,Dalmonego, Giulio

, p. 1541 - 1546 (2007/10/03)

N-alkyl-substituted prop-2-yn-1-amines and N-tri-, tetra- and penta-alkyl-substituted guanidines or other strong organic bases assemble under the action of carbon dioxide to afford carbamates, from which methyleneoxazolidinones 2 are formed by ring closure. If alkyl or cycloalkyl chains of appropriate length are present in the guanidines the reaction readily occurs under heterogenous conditions without solvent.

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