Cas 1357256-77-9,3-(2-chlorophenyl)-4-phenyl-5-benzyl-1,3,4,5,5a,6,7,8,9,9a-decahydro-isoxazolo[4,3-c]quinoline

1357256-77-9

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Basic information

Product Name: 3-(2-chlorophenyl)-4-phenyl-5-benzyl-1,3,4,5,5a,6,7,8,9,9a-decahydro-isoxazolo[4,3-c]quinoline
Synonyms: 3-(2-chlorophenyl)-4-phenyl-5-benzyl-1,3,4,5,5a,6,7,8,9,9a-decahydro-isoxazolo[4,3-c]quinoline
CAS NO:1357256-77-9
Molecular Formula:
Molecular Weight: 457.015
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: 3-(2-chlorophenyl)-4-phenyl-5-benzyl-1,3,4,5,5a,6,7,8,9,9a-decahydro-isoxazolo[4,3-c]quinoline(CAS DataBase Reference)
NIST Chemistry Reference: 3-(2-chlorophenyl)-4-phenyl-5-benzyl-1,3,4,5,5a,6,7,8,9,9a-decahydro-isoxazolo[4,3-c]quinoline(1357256-77-9)
EPA Substance Registry System: 3-(2-chlorophenyl)-4-phenyl-5-benzyl-1,3,4,5,5a,6,7,8,9,9a-decahydro-isoxazolo[4,3-c]quinoline(1357256-77-9)

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: 1357256-77-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1357256-77-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,7,2,5 and 6 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1357256-77:
(9*1)+(8*3)+(7*5)+(6*7)+(5*2)+(4*5)+(3*6)+(2*7)+(1*7)=179
179 % 10 = 9
So 1357256-77-9 is a valid CAS Registry Number.

1357256-77-9Upstream product

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1357256-77-9Relevant academic research and scientific papers

Isoxazoles incorporated N-substituted decahydroquinolines: A precursor to the next generation antimicrobial drug

Babu, Mariappan,Pitchumani, Kasi,Ramesh, Penugonda

, p. 608 - 614 (2012/03/10)

We report here a simple entry into N-substituted decahydroisoxazoloquinoline system with substituents at position 3 and 4 from the readily available substrates for the first time. The synthesized isoxazoloquinolines were evaluated against six bacterial an

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