Cas 1450908-77-6,(S)-ethyl 1-(4-methoxyphenyl)-6-methyl-4-pentyl-1,4-dihydropyridazine-3-carboxylate

1450908-77-6

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Basic information

Product Name: (S)-ethyl 1-(4-methoxyphenyl)-6-methyl-4-pentyl-1,4-dihydropyridazine-3-carboxylate
Synonyms: (S)-ethyl 1-(4-methoxyphenyl)-6-methyl-4-pentyl-1,4-dihydropyridazine-3-carboxylate
CAS NO:1450908-77-6
Molecular Formula:
Molecular Weight: 344.454
EINECS: N/A
Product Categories: N/A
Mol File: 1450908-77-6.mol
Article Data: 1

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: (S)-ethyl 1-(4-methoxyphenyl)-6-methyl-4-pentyl-1,4-dihydropyridazine-3-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (S)-ethyl 1-(4-methoxyphenyl)-6-methyl-4-pentyl-1,4-dihydropyridazine-3-carboxylate(1450908-77-6)
EPA Substance Registry System: (S)-ethyl 1-(4-methoxyphenyl)-6-methyl-4-pentyl-1,4-dihydropyridazine-3-carboxylate(1450908-77-6)

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: 1450908-77-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1450908-77-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,0,9,0 and 8 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1450908-77:
(9*1)+(8*4)+(7*5)+(6*0)+(5*9)+(4*0)+(3*8)+(2*7)+(1*7)=166
166 % 10 = 6
So 1450908-77-6 is a valid CAS Registry Number.

1450908-77-6Upstream product

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1450908-77-6Relevant articles and documents

Catalytic asymmetric construction of chiral hydropyridazines via conjugate addition of N-monosubstituted hydrazones to enones

Wu, Wenbin,Yuan, Xiaoqian,Hu, Juan,Wu, Xinxin,Wei, Yuan,Liu, Zunwu,Lu, Junzhu,Ye, Jinxing

, p. 4524 - 4527 (2013/09/24)

The first example of a highly enantioselective and scalable formal diaza-ene reaction between N-monosubstituted hydrazones and enones catalyzed by a simple chiral primary-second diamine salt has been developed. The catalytic process provides a highly prac

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