Cas 1438276-61-9,(6S,6aR,10aR)-7-amino-2-chloro-10-methyl-6a-nitro-6,9-diphenyl-6a,10a-dihydro-6H-benzo[c]chromene-8-carbonitrile

1438276-61-9

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Basic information

Product Name: (6S,6aR,10aR)-7-amino-2-chloro-10-methyl-6a-nitro-6,9-diphenyl-6a,10a-dihydro-6H-benzo[c]chromene-8-carbonitrile
Synonyms:
CAS NO:1438276-61-9
Molecular Formula:
Molecular Weight: 469.927
EINECS: N/A
Product Categories: N/A
Mol File: 1438276-61-9.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: (6S,6aR,10aR)-7-amino-2-chloro-10-methyl-6a-nitro-6,9-diphenyl-6a,10a-dihydro-6H-benzo[c]chromene-8-carbonitrile(CAS DataBase Reference)
NIST Chemistry Reference: (6S,6aR,10aR)-7-amino-2-chloro-10-methyl-6a-nitro-6,9-diphenyl-6a,10a-dihydro-6H-benzo[c]chromene-8-carbonitrile(1438276-61-9)
EPA Substance Registry System: (6S,6aR,10aR)-7-amino-2-chloro-10-methyl-6a-nitro-6,9-diphenyl-6a,10a-dihydro-6H-benzo[c]chromene-8-carbonitrile(1438276-61-9)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1438276-61-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1438276-61-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,8,2,7 and 6 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1438276-61:
(9*1)+(8*4)+(7*3)+(6*8)+(5*2)+(4*7)+(3*6)+(2*6)+(1*1)=179
179 % 10 = 9
So 1438276-61-9 is a valid CAS Registry Number.

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1438276-61-9Relevant articles and documents

Construction of chiral multi-functionalized polyheterocyclic benzopyran derivatives by using an asymmetric organocatalytic domino reaction

Guo, Zhi-Wei,Li, Xin-Sheng,Zhu, Wei-Dong,Xie, Jian-Wu

, p. 6924 - 6932 (2013/03/29)

The asymmetric domino reaction of various α,α-dicyano olefins to 3-nitro-2H-chromenes was studied employing readily available cinchona-derived bifunctional thioureas as organocatalysts. These new transformations were highly regio-, chemo-, diastereo-, and

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