Cas 1356685-91-0,(1S,4R)-4-(5-(benzyloxy)-1-ethoxy-2-(ethoxycarbonyl)-1-oxopentan-2-yl)cyclobut-2-enecarboxylic acid

1356685-91-0

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Basic information

Product Name: (1S,4R)-4-(5-(benzyloxy)-1-ethoxy-2-(ethoxycarbonyl)-1-oxopentan-2-yl)cyclobut-2-enecarboxylic acid
Synonyms: (1S,4R)-4-(5-(benzyloxy)-1-ethoxy-2-(ethoxycarbonyl)-1-oxopentan-2-yl)cyclobut-2-enecarboxylic acid
CAS NO:1356685-91-0
Molecular Formula:
Molecular Weight: 404.46
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: (1S,4R)-4-(5-(benzyloxy)-1-ethoxy-2-(ethoxycarbonyl)-1-oxopentan-2-yl)cyclobut-2-enecarboxylic acid(CAS DataBase Reference)
NIST Chemistry Reference: (1S,4R)-4-(5-(benzyloxy)-1-ethoxy-2-(ethoxycarbonyl)-1-oxopentan-2-yl)cyclobut-2-enecarboxylic acid(1356685-91-0)
EPA Substance Registry System: (1S,4R)-4-(5-(benzyloxy)-1-ethoxy-2-(ethoxycarbonyl)-1-oxopentan-2-yl)cyclobut-2-enecarboxylic acid(1356685-91-0)

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: 1356685-91-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1356685-91-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,6,6,8 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1356685-91:
(9*1)+(8*3)+(7*5)+(6*6)+(5*6)+(4*8)+(3*5)+(2*9)+(1*1)=200
200 % 10 = 0
So 1356685-91-0 is a valid CAS Registry Number.

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1356685-91-0Relevant academic research and scientific papers

Catalytic asymmetric diastereodivergent deracemization

Luparia, Marco,Oliveira, Maria Teresa,Audisio, Davide,Frebault, Frederic,Goddard, Richard,Maulide, Nuno

, p. 12631 - 12635 (2011)

Your wish is my command: Deracemization is a powerful strategy wherein a racemate is converted into a 100 % yield of a single enantiopure product. A new concept in catalytic deracemization is presented, in which a racemate with n stereogenic elements can be selectively converted into each one of 2m (m=number of chiral centers of the product) different enantiopure products, by simple tuning of the reaction conditions. Copyright

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