Cas 918159-87-2,(3S)-(-)-1-di(p-anisyl)methyl-7-chloro-1,3-dihydro-5-phenyl-3-(2-thiomethyl)ethyl-2H-1,4-benzodiazepin-2-one

918159-87-2

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Basic information

Product Name: (3S)-(-)-1-di(p-anisyl)methyl-7-chloro-1,3-dihydro-5-phenyl-3-(2-thiomethyl)ethyl-2H-1,4-benzodiazepin-2-one
Synonyms: (3S)-(-)-1-di(p-anisyl)methyl-7-chloro-1,3-dihydro-5-phenyl-3-(2-thiomethyl)ethyl-2H-1,4-benzodiazepin-2-one
CAS NO:918159-87-2
Molecular Formula:
Molecular Weight: 571.14
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: (3S)-(-)-1-di(p-anisyl)methyl-7-chloro-1,3-dihydro-5-phenyl-3-(2-thiomethyl)ethyl-2H-1,4-benzodiazepin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (3S)-(-)-1-di(p-anisyl)methyl-7-chloro-1,3-dihydro-5-phenyl-3-(2-thiomethyl)ethyl-2H-1,4-benzodiazepin-2-one(918159-87-2)
EPA Substance Registry System: (3S)-(-)-1-di(p-anisyl)methyl-7-chloro-1,3-dihydro-5-phenyl-3-(2-thiomethyl)ethyl-2H-1,4-benzodiazepin-2-one(918159-87-2)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 918159-87-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 918159-87-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,8,1,5 and 9 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 918159-87:
(8*9)+(7*1)+(6*8)+(5*1)+(4*5)+(3*9)+(2*8)+(1*7)=202
202 % 10 = 2
So 918159-87-2 is a valid CAS Registry Number.

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918159-87-2Relevant academic research and scientific papers

Enantioselective synthesis of diversely substituted quaternary 1,4-benzodiazepin-2-ones and 1,4-benzodiazepine-2,5-diones

Carlier, Paul R.,Zhao, Hongwu,MacQuarrie-Hunter, Stephanie L.,DeGuzman, Joseph C.,Hsu, Danny C.

, p. 15215 - 15220 (2007/10/03)

Benzodiazepines are privileged scaffolds in medicinal chemistry, but enantiopure examples containing quaternary stereogenic centers are extremely rare. We demonstrate that installation of the di-(p-anisyl)methyl (DAM) group at N1 of 1,4-benzodiazepin-2-on

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