19293-63-1

Basic information

• Product Name: 1,1-dicyclohexylmethanamine
• Synonyms: 1,1-Dicyclohexylmethanamine; cyclohexanemethanamine, α-cyclohexyl-
• CAS NO: 19293-63-1
• Molecular Formula: C₁₃H₂₅N
• Molecular Weight: 195.3443
• Mol File: 19293-63-1.mol

Chemical Properties

• Boiling Point: 273.124°C at 760 mmHg
• Flash Point: 114.926°C
• Density: 0.938g/cm³
• Vapor Pressure: 0.006mmHg at 25°C
• Refractive Index: 1.502
• CAS DataBase Reference: 1,1-dicyclohexylmethanamine(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1-dicyclohexylmethanamine(19293-63-1)
• EPA Substance Registry System: 1,1-dicyclohexylmethanamine(19293-63-1)

Safety Data

• Hazardous Substances Data: 19293-63-1(Hazardous Substances Data)

Usage

Synonyms

DCHMA

Type of compound

Organic compound

Classification

Tertiary amine

Primary use

Curing agent or catalyst in the production of epoxy resins

Boiling point

High

Vapor pressure

Low

Suitability

High-temperature applications

Odor

Strong

Hazardous nature

Inhalation or ingestion can be hazardous

Additional use

Reagent in organic synthesis for various chemical reactions

Importance

Plays a significant role in the production of epoxy resins and organic synthesis

Safety precautions

Should be handled with caution due to potential health hazards

Upstream product

• 6316-03-6 dicyclohexyl ketone oxime 
• 119-60-8 dicyclohexyl ketone 
• 220047-49-4 dicyclohexylmethyl isocyanate 

Downstream Products

• 1025999-81-8 (1S,3aS,3bS,9aR,9bS,11aS)-1-(Dicyclohexylmethyl-carbamoyl)-9a,11a-dimethyl-7-oxo-1,2,3,3a,3b,4,7,8,9,9a,9b,10,11,11a-tetradecahydro-cyclopenta[i]phenanthridine-5-carboxylic acid tert-butyl ester 
• 365282-02-6 4-benzylsulfanyl-2-[[(dicyclohexylmethyl-carbamoyl)-methyl]-(4-methoxy-benzenesulfonyl)-amino]-butyric acid methyl ester 
• 709024-86-2 1-dicyclohexylmethyl-piperidin-4-one 
• 1027717-63-0 3,5-bis(trifluoromethyl)cinnamonitrile 
• 705250-77-7 3-[3,5-bis(trifluoromethyl)phenyl]-2(Z)-propenoic acid methyl ester 
• 91-63-4 2-methylquinoline 
• 1730-91-2 (S)-2-Methylbutyric acid 
• 116-53-0 2-Methylbutanoic acid 
• 32231-50-8 (R)-2-methylbutyric acid 
• 22204-53-1 (2S)-2-(6-methoxy(2-naphthyl))propanoic acid 
• 33689-28-0 cyclobutane-1,2-dione 
• 1072879-56-1 N-benzylidene-1,1-dicyclohexylmethanamine 

Relevant articles and documents

KINASE INHIBITORS AND METHOD OF TREATING CANCER WITH SAME

The present teachings provide a compound represented by Structural Formula (I): or a pharmaceutically acceptable salt thereof. Also described are a pharmaceutical composition and method of use thereof.

BICYCLIC HETEROCYCLE DERIVATIVES AND USE THEREOF AS GPR119 MODULATORS

The present invention relates to Bicyclic Heterocycle Derivatives of formula (I), compositions comprising a Bicyclic Heterocycle Derivative, and methods of using the Bicyclic Heterocycle Derivatives for treating or preventing obesity, diabetes, a metabolic disorder, a cardiovascular disease or a disorder related to the activity of GPR1 19 in a patient.

Mapping the active site in a chemzyme: Diversity in the N-substituent in the catalytic asymmetric aziridination of imines

(Chemical Equation Presented) The active site of the aziridination catalyst derived from either the VANOL or VAPOL ligand and B(OPh)3 is larger than expected and can accommodate not only significant substitution on the diarylmethyl unit of the imine but also that alkyl (but not perfluorylalkyl) substituents on the aryl groups lead to enhanced rates and enantioselection. The screen of diarylmethyl N-substituents on the imine revealed that the 3,5-di-tert-butyldianisylmethyl group (BUDAM) gave exceptionally high asymmetric inductions for imines of aryl aldehydes.

Matrix metalloproteinase inhibitors

A compound, which is an amine derivative of formula (I) wherein W is —CNHOH or —COOH: R1and R2are each hydrogen or an organic residue, R3is an organic group, Q is a secondary or tertiary acyclic or cyclic amido group, and

Atroposelectivity in the reactions of ortholithiated aromatic tertiary amides with aldehydes

The products of the addition of ortholithiated N,N-dialkylnaphthamides to aldehydes are pairs of stable, diastereoisomeric atropisomers, formed with selectivities of up to 90:10 in favour of the syn-atropisomer.