Cas 40235-36-7,methyl 5-(4-(dimethylamino)phenyl)-1H-1,2,3-triazole-4-carboxylate

40235-36-7

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Basic information

Product Name: methyl 5-(4-(dimethylamino)phenyl)-1H-1,2,3-triazole-4-carboxylate
Synonyms: methyl 5-(4-(dimethylamino)phenyl)-1H-1,2,3-triazole-4-carboxylate
CAS NO:40235-36-7
Molecular Formula:
Molecular Weight: 246.269
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: methyl 5-(4-(dimethylamino)phenyl)-1H-1,2,3-triazole-4-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: methyl 5-(4-(dimethylamino)phenyl)-1H-1,2,3-triazole-4-carboxylate(40235-36-7)
EPA Substance Registry System: methyl 5-(4-(dimethylamino)phenyl)-1H-1,2,3-triazole-4-carboxylate(40235-36-7)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 40235-36-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 40235-36-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,2,3 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 40235-36:
(7*4)+(6*0)+(5*2)+(4*3)+(3*5)+(2*3)+(1*6)=77
77 % 10 = 7
So 40235-36-7 is a valid CAS Registry Number.

40235-36-7Upstream product

55420-26-3 (Z)-2-bromo-3-(4-(dimethylamino)phenyl)acrylic acid methyl ester

40235-36-7Downstream Products

40235-36-7Relevant academic research and scientific papers

α-Haloacrylates as acceptors in the [3 + 2] cycloaddition reaction with NaN3: An expedient approach to N-unsubstituted 1,2,3-triazole-4-carboxylates

Augustine, John Kallikat,Boodappa, Chandrakantha,Venkatachaliah, Srinivasa

, p. 2280 - 2288 (2014/04/03)

An expedient synthesis of N-unsubstituted 1,2,3-triazole-4-carboxylates has been demonstrated through [3 + 2] cycloaddition of sodium azide with α-haloacrylates. The process is highly reliable and exhibits an unusually wide scope with respect to α-fluoro-

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