Cas 1284151-72-9,4-benzyl-1-(3,5-dichlorophenyl)-2-[3-(trifluoromethyl)benzyl]-2,3,4,5-tetrahydro-1H-benzo[e][1,4]diazepine

1284151-72-9

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Basic information

Product Name: 4-benzyl-1-(3,5-dichlorophenyl)-2-[3-(trifluoromethyl)benzyl]-2,3,4,5-tetrahydro-1H-benzo[e][1,4]diazepine
Synonyms: 4-benzyl-1-(3,5-dichlorophenyl)-2-[3-(trifluoromethyl)benzyl]-2,3,4,5-tetrahydro-1H-benzo[e][1,4]diazepine
CAS NO:1284151-72-9
Molecular Formula:
Molecular Weight: 541.443
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: 4-benzyl-1-(3,5-dichlorophenyl)-2-[3-(trifluoromethyl)benzyl]-2,3,4,5-tetrahydro-1H-benzo[e][1,4]diazepine(CAS DataBase Reference)
NIST Chemistry Reference: 4-benzyl-1-(3,5-dichlorophenyl)-2-[3-(trifluoromethyl)benzyl]-2,3,4,5-tetrahydro-1H-benzo[e][1,4]diazepine(1284151-72-9)
EPA Substance Registry System: 4-benzyl-1-(3,5-dichlorophenyl)-2-[3-(trifluoromethyl)benzyl]-2,3,4,5-tetrahydro-1H-benzo[e][1,4]diazepine(1284151-72-9)

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: 1284151-72-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1284151-72-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,4,1,5 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1284151-72:
(9*1)+(8*2)+(7*8)+(6*4)+(5*1)+(4*5)+(3*1)+(2*7)+(1*2)=149
149 % 10 = 9
So 1284151-72-9 is a valid CAS Registry Number.

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1284151-72-9Relevant academic research and scientific papers

Synthesis of saturated 1,4-benzodiazepines via Pd-catalyzed carboamination reactions.

Neukom, Joshua D.,Aquino, Alvin S.,Wolfe, John P.

, p. 2196 - 2199 (2011/06/25)

Chemical equations presented. A new synthesis of 1,4-benzodiazepines and 1,4-benzodiazepin-5-ones is reported. The Pd-catalyzed coupling of N-allyl-2-aminobenzylamine derivatives with aryl bromides affords the heterocyclic products in good yield, and substrates bearing allylic methyl groups are transformed to cis-2,3-disubstituted products with >20:1 dr.

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