Cas 1285535-58-1,benzyl 2-{3-amino-5-[4-methyl-6-(5-methyl-1,2,4-oxadiazol-3-yl)-4-phenyl-2,3-dihydro-1H-quinolin-3-yl]phenyl}-5-carbamoylbenzoate

1285535-58-1

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Basic information

Product Name: benzyl 2-{3-amino-5-[4-methyl-6-(5-methyl-1,2,4-oxadiazol-3-yl)-4-phenyl-2,3-dihydro-1H-quinolin-3-yl]phenyl}-5-carbamoylbenzoate
Synonyms: benzyl 2-{3-amino-5-[4-methyl-6-(5-methyl-1,2,4-oxadiazol-3-yl)-4-phenyl-2,3-dihydro-1H-quinolin-3-yl]phenyl}-5-carbamoylbenzoate
CAS NO:1285535-58-1
Molecular Formula:
Molecular Weight: 649.749
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: benzyl 2-{3-amino-5-[4-methyl-6-(5-methyl-1,2,4-oxadiazol-3-yl)-4-phenyl-2,3-dihydro-1H-quinolin-3-yl]phenyl}-5-carbamoylbenzoate(CAS DataBase Reference)
NIST Chemistry Reference: benzyl 2-{3-amino-5-[4-methyl-6-(5-methyl-1,2,4-oxadiazol-3-yl)-4-phenyl-2,3-dihydro-1H-quinolin-3-yl]phenyl}-5-carbamoylbenzoate(1285535-58-1)
EPA Substance Registry System: benzyl 2-{3-amino-5-[4-methyl-6-(5-methyl-1,2,4-oxadiazol-3-yl)-4-phenyl-2,3-dihydro-1H-quinolin-3-yl]phenyl}-5-carbamoylbenzoate(1285535-58-1)

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: 1285535-58-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1285535-58-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,5,5,3 and 5 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1285535-58:
(9*1)+(8*2)+(7*8)+(6*5)+(5*5)+(4*3)+(3*5)+(2*5)+(1*8)=181
181 % 10 = 1
So 1285535-58-1 is a valid CAS Registry Number.

1285535-58-1Upstream product

1285535-56-9 C₄₀H₃₃N₅O₆

1285535-58-1Downstream Products

1285535-58-1Relevant academic research and scientific papers

An efficient method for aryl nitro reduction and cleavage of azo compounds using iron powder/calcium chloride

Chandrappa,Vinaya,Ramakrishnappa,Rangappa

, p. 3019 - 3022 (2010)

A novel, efficient Fe/CaCl2 system is revealed for the reduction of nitroarenes and reductive cleavage of azo compounds by catalytic transfer hydrogenation (CTH). The selective reduction of nitro compounds in the presence of sensitive functional groups including halides, carbonyl, hydroxyl, aldehyde, methyl, methoxy, acetyl, nitrile, and ester substituents with an excellent yields is reported. The simple experimental procedure and easy purification make the protocol advantageous

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