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1,3-Di-p-tolylcarbodiimide_Molecular_structure_CAS_726-42-1)
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1,3-Di-p-tolylcarbodiimide

Catalog No. D219800 Name Sigma Aldrich
CAS Number 726-42-1 Website http://www.sigmaaldrich.com
M. F. C15H14N2 Telephone 1-800-521-8956
M. W. 222.28506 Fax
Purity 96% Email
Storage Chembase ID: 148781

SYNONYMS

Title
1,3-二对甲苯基碳二酰亚胺
IUPAC name
4-methyl-N-[N-(4-methylphenyl)carboximidoyl]aniline
IUPAC Traditional name
di-p-tolylcarbodiimide
Synonyms
Bis(4-methylphenyl)carbodiimide
NSC 20627
N,N′-Methanetetraylbis[4-methyl]benzenamine

DATABASE IDS

CAS Number 726-42-1
EC Number 211-971-7
PubChem SID 24893653
MDL Number MFCD00010701

PROPERTIES

Linear Formula CH3C6H4N=C=NC6H4CH3
Purity 96%
Boiling Point 221-223 °C/20 mmHg(lit.)
Melting Point 56-58 °C(lit.)
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H302-H312-H315-H319-H332-H335
European Hazard Symbols Harmful Harmful (Xn)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements P261-P280-P305 + P351 + P338
Risk Statements 20/21/22-36/37/38
Safety Statements 26-37/39
Storage Temperature 2-8°C
German water hazard class 3

DETAILS

Description (English)
Packaging
1, 5 g in glass bottle
Application
Reactant for synthesis of:
• Cyclic guanidines1
• Five membered heterometallacycloallenes2
• Benzimidazoles or quinazolines via nucleophilic addition and intramolecular C-C bond formation3
• Benzoxazole and benzimidazole derivatives via cross-coupling reactions4
• Gem-difluorodihydrouracil derivatives via addition reactions5Reactant for ketene cycloadditions6
Description (简体中文)
包装
1, 5 g in glass bottle
Application
Reactant for synthesis of:
• Cyclic guanidines1
• Five membered heterometallacycloallenes2
• Benzimidazoles or quinazolines via nucleophilic addition and intramolecular C-C bond formation3
• Benzoxazole and benzimidazole derivatives via cross-coupling reactions4
• Gem-difluorodihydrouracil derivatives via addition reactions5Reactant for ketene cycloadditions6

REFERENCES