Cas 1003570-07-7,ethyl (3S,4R)-3-(tert-butyldiphenylsiloxy)-4-methyl-5-oxocyclopent-1-enecarboxylate

1003570-07-7

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Basic information

Product Name: ethyl (3S,4R)-3-(tert-butyldiphenylsiloxy)-4-methyl-5-oxocyclopent-1-enecarboxylate
Synonyms: ethyl (3S,4R)-3-(tert-butyldiphenylsiloxy)-4-methyl-5-oxocyclopent-1-enecarboxylate
CAS NO:1003570-07-7
Molecular Formula:
Molecular Weight: 422.596
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: ethyl (3S,4R)-3-(tert-butyldiphenylsiloxy)-4-methyl-5-oxocyclopent-1-enecarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl (3S,4R)-3-(tert-butyldiphenylsiloxy)-4-methyl-5-oxocyclopent-1-enecarboxylate(1003570-07-7)
EPA Substance Registry System: ethyl (3S,4R)-3-(tert-butyldiphenylsiloxy)-4-methyl-5-oxocyclopent-1-enecarboxylate(1003570-07-7)

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: 1003570-07-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1003570-07-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,3,5,7 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1003570-07:
(9*1)+(8*0)+(7*0)+(6*3)+(5*5)+(4*7)+(3*0)+(2*0)+(1*7)=87
87 % 10 = 7
So 1003570-07-7 is a valid CAS Registry Number.

1003570-07-7Upstream product

1003570-06-6 ethyl (4R,5S)-5-(tert-butyldiphenylsiloxy)-2-(Z/E)-ethylidene-4-methyl-3-oxohept-6-enoate

1003570-07-7Downstream Products

1003570-07-7Relevant academic research and scientific papers

Dramatic solvent effect on the diastereoselectivity of Michael addition: Study toward the synthesis of the ABC ring system of hexacyclinic acid

Toueg, Julie,Prunet, Joelle

, p. 45 - 48 (2008/09/17)

During our studies toward the synthesis of the ABC ring system of hexacyclinic acid, we have observed a dramatic influence of the solvent on both our key steps. The diastereoselectivity of the intermolecular Michael addition could be totally reversed by c

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