Cas 1356935-68-6,2-((1R,2S,3R,4R)-3-(2,5-dimethoxyphenyl)-2-nitro-4-phenylcyclobutyl)acetaldehyde

1356935-68-6

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Basic information

Product Name: 2-((1R,2S,3R,4R)-3-(2,5-dimethoxyphenyl)-2-nitro-4-phenylcyclobutyl)acetaldehyde
Synonyms: 2-((1R,2S,3R,4R)-3-(2,5-dimethoxyphenyl)-2-nitro-4-phenylcyclobutyl)acetaldehyde
CAS NO:1356935-68-6
Molecular Formula:
Molecular Weight: 355.39
EINECS: N/A
Product Categories: N/A
Mol File: 1356935-68-6.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: 2-((1R,2S,3R,4R)-3-(2,5-dimethoxyphenyl)-2-nitro-4-phenylcyclobutyl)acetaldehyde(CAS DataBase Reference)
NIST Chemistry Reference: 2-((1R,2S,3R,4R)-3-(2,5-dimethoxyphenyl)-2-nitro-4-phenylcyclobutyl)acetaldehyde(1356935-68-6)
EPA Substance Registry System: 2-((1R,2S,3R,4R)-3-(2,5-dimethoxyphenyl)-2-nitro-4-phenylcyclobutyl)acetaldehyde(1356935-68-6)

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: 1356935-68-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1356935-68-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,6,9,3 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1356935-68:
(9*1)+(8*3)+(7*5)+(6*6)+(5*9)+(4*3)+(3*5)+(2*6)+(1*8)=196
196 % 10 = 6
So 1356935-68-6 is a valid CAS Registry Number.

1356935-68-6Upstream product

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1356935-68-6Relevant articles and documents

Asymmetric organocatalytic formal [2 + 2]-cycloadditions via bifunctional H-bond directing dienamine catalysis

Albrecht, Lukasz,Dickmeiss, Gustav,Acosta, Fabio Cruz,Rodriguez-Escrich, Carles,Davis, Rebecca L.,Jorgensen, Karl Anker

supporting information; experimental part, p. 2543 - 2546 (2012/04/04)

A new concept in organocatalysis allowing for the construction of cyclobutanes with four contiguous stereocenters with complete diastereo-and enantiomeric control by a formal [2 + 2]-cycloaddition is presented. The concept is based on simultaneous dual ac

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