Cas 1436787-99-3,(1R,2R,3R,4R,4aS,8aS)-8a-hydroxy-3-nitro-4-phenyl-2-(thiophen-2-yl)decahydronaphthalene-1-carbaldehyde

1436787-99-3

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Basic information

Product Name: (1R,2R,3R,4R,4aS,8aS)-8a-hydroxy-3-nitro-4-phenyl-2-(thiophen-2-yl)decahydronaphthalene-1-carbaldehyde
Synonyms: (1R,2R,3R,4R,4aS,8aS)-8a-hydroxy-3-nitro-4-phenyl-2-(thiophen-2-yl)decahydronaphthalene-1-carbaldehyde
CAS NO:1436787-99-3
Molecular Formula:
Molecular Weight: 385.484
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: (1R,2R,3R,4R,4aS,8aS)-8a-hydroxy-3-nitro-4-phenyl-2-(thiophen-2-yl)decahydronaphthalene-1-carbaldehyde(CAS DataBase Reference)
NIST Chemistry Reference: (1R,2R,3R,4R,4aS,8aS)-8a-hydroxy-3-nitro-4-phenyl-2-(thiophen-2-yl)decahydronaphthalene-1-carbaldehyde(1436787-99-3)
EPA Substance Registry System: (1R,2R,3R,4R,4aS,8aS)-8a-hydroxy-3-nitro-4-phenyl-2-(thiophen-2-yl)decahydronaphthalene-1-carbaldehyde(1436787-99-3)

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: 1436787-99-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1436787-99-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,6,7,8 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1436787-99:
(9*1)+(8*4)+(7*3)+(6*6)+(5*7)+(4*8)+(3*7)+(2*9)+(1*9)=213
213 % 10 = 3
So 1436787-99-3 is a valid CAS Registry Number.

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1436787-99-3Relevant academic research and scientific papers

Achiral co-catalyst induced switches in catalytic asymmetric reactions on racemic mixtures (RRM): From stereodivergent RRM to stereoconvergent deracemization by combination of hydrogen bond donating and chiral amine catalysts

Ma, Guangning,Lin, Shuangzheng,Ibrahem, Ismail,Kubik, Grzegorz,Liu, Leifeng,Sun, Junliang,Cordova, Armando

, p. 2865 - 2872 (2013/01/15)

A stereochemical divergent approach for the highly enantioselective synthesis of distinct bicyclic products with multiple stereocenters from a racemate using a single chiral catalyst is disclosed. It is based on switches of the overall reaction pathways i

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