Cas 866871-73-0,N-(2,4-dimethylphenyl)-5-methyl-1-phenyl-1H-1,2,3-triazole-4-carboxamide

866871-73-0

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Basic information

Product Name: N-(2,4-dimethylphenyl)-5-methyl-1-phenyl-1H-1,2,3-triazole-4-carboxamide
Synonyms: N-(2,4-dimethylphenyl)-5-methyl-1-phenyl-1H-1,2,3-triazole-4-carboxamide
CAS NO:866871-73-0
Molecular Formula: C₁₈H₁₈N₄O
Molecular Weight: 306.36172
EINECS: N/A
Product Categories: N/A
Mol File: 866871-73-0.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: N-(2,4-dimethylphenyl)-5-methyl-1-phenyl-1H-1,2,3-triazole-4-carboxamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(2,4-dimethylphenyl)-5-methyl-1-phenyl-1H-1,2,3-triazole-4-carboxamide(866871-73-0)
EPA Substance Registry System: N-(2,4-dimethylphenyl)-5-methyl-1-phenyl-1H-1,2,3-triazole-4-carboxamide(866871-73-0)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 866871-73-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 866871-73-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,6,8,7 and 1 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 866871-73:
(8*8)+(7*6)+(6*6)+(5*8)+(4*7)+(3*1)+(2*7)+(1*3)=230
230 % 10 = 0
So 866871-73-0 is a valid CAS Registry Number.

866871-73-0Upstream product

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866871-73-0Relevant academic research and scientific papers

Organocatalytic 1,3-Dipolar Cycloaddition Reaction of β-Keto Amides with Azides - Direct Access to 1,4,5-Trisubstituted 1,2,3-Triazole-4-carboxamides

Zhou, Xiao,Xu, Xianhong,Liu, Kun,Gao, Hua,Wang, Wei,Li, Wenjun

supporting information, p. 1886 - 1890 (2016/05/09)

Organocatalytic [3+2] 1,3-dipolar cycloaddition reactions of β-keto amides with azides catalyzed by 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) have been developed. This strategy generates 1,4,5-trisubstituted 1,2,3-triazole-4-carboxamides in high yields and

Synthetic method of 1,4,5-trisubstituted-1,2,3-triazole compound

-

Paragraph 0036, (2016/10/07)

The invention discloses a synthetic method of a 1,4,5-trisubstituted-1,2,3-triazole compound. In a reaction solvent, acetoacetamide and nitrine are used as reaction materials and Lewis base is used as a catalyst to carry out a reaction so as to obtain a p

Intramolecular hydrogen bonding-assisted cyclocondensation of α-diazoketones with various amines: A strategy for highly efficient Wolff 1,2,3-triazole synthesis

Wang, Zikun,Bi, Xihe,Liao, Peiqiu,Zhang, Rui,Liang, Yongjiu,Dong, Dewen

, p. 7076 - 7078 (2012/08/14)

A catalytic and highly efficient Wolff's cyclocondensation of α-diazoketones with aromatic and aliphatic amines has been realized for the first time by utilizing the strategy of an intramolecular hydrogen bonding-activating carbonyl group. This approach successfully solved the challenging problem of poor condensation efficiency in Wolff 1,2,3-triazole synthesis, and constitutes a powerful method for the synthesis of highly functionalized 1,2,3-triazoles. The Royal Society of Chemistry 2012.

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