Cas 1242077-08-2,(E)-4-phenyl-1-(4-(3,4,5-trimethoxyphenyl)but-3-en-2-yl)-1H-1,2,3-triazole

1242077-08-2

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Basic information

Product Name: (E)-4-phenyl-1-(4-(3,4,5-trimethoxyphenyl)but-3-en-2-yl)-1H-1,2,3-triazole
Synonyms: (E)-4-phenyl-1-(4-(3,4,5-trimethoxyphenyl)but-3-en-2-yl)-1H-1,2,3-triazole
CAS NO:1242077-08-2
Molecular Formula:
Molecular Weight: 365.432
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: (E)-4-phenyl-1-(4-(3,4,5-trimethoxyphenyl)but-3-en-2-yl)-1H-1,2,3-triazole(CAS DataBase Reference)
NIST Chemistry Reference: (E)-4-phenyl-1-(4-(3,4,5-trimethoxyphenyl)but-3-en-2-yl)-1H-1,2,3-triazole(1242077-08-2)
EPA Substance Registry System: (E)-4-phenyl-1-(4-(3,4,5-trimethoxyphenyl)but-3-en-2-yl)-1H-1,2,3-triazole(1242077-08-2)

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: 1242077-08-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1242077-08-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,2,0,7 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1242077-08:
(9*1)+(8*2)+(7*4)+(6*2)+(5*0)+(4*7)+(3*7)+(2*0)+(1*8)=122
122 % 10 = 2
So 1242077-08-2 is a valid CAS Registry Number.

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1242077-08-2Relevant academic research and scientific papers

Efficient synthesis of allylic azides and one-pot regioselective synthesis of 1,4-disubstituted 1,2,3-triazoles from homoallyl alcohols

Surendra Reddy,Ravi,Sreedhar

experimental part, p. 4037 - 4041 (2010/08/07)

This protocol is for an expedient and operationally simple synthesis of allylic azides and one-pot synthesis of 1,4-disubstituted 1,2,3-triazoles from homoallyl alcohols. Synthesis of allylic azides involves the palladium-catalyzed hydroazidation of unact

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