Cas 1315554-21-2,(4S,5R,E)-methyl 5-(cyclopent-1-en-1-yl)-5-methoxy-4-(4-methoxyphenyl)pent-2-enoate

1315554-21-2

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Basic information

Product Name: (4S,5R,E)-methyl 5-(cyclopent-1-en-1-yl)-5-methoxy-4-(4-methoxyphenyl)pent-2-enoate
Synonyms: (4S,5R,E)-methyl 5-(cyclopent-1-en-1-yl)-5-methoxy-4-(4-methoxyphenyl)pent-2-enoate
CAS NO:1315554-21-2
Molecular Formula:
Molecular Weight: 316.397
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: (4S,5R,E)-methyl 5-(cyclopent-1-en-1-yl)-5-methoxy-4-(4-methoxyphenyl)pent-2-enoate(CAS DataBase Reference)
NIST Chemistry Reference: (4S,5R,E)-methyl 5-(cyclopent-1-en-1-yl)-5-methoxy-4-(4-methoxyphenyl)pent-2-enoate(1315554-21-2)
EPA Substance Registry System: (4S,5R,E)-methyl 5-(cyclopent-1-en-1-yl)-5-methoxy-4-(4-methoxyphenyl)pent-2-enoate(1315554-21-2)

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: 1315554-21-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1315554-21-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,5,5,5 and 4 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1315554-21:
(9*1)+(8*3)+(7*1)+(6*5)+(5*5)+(4*5)+(3*4)+(2*2)+(1*1)=132
132 % 10 = 2
So 1315554-21-2 is a valid CAS Registry Number.

1315554-21-2Upstream product

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1315554-21-2Relevant academic research and scientific papers

Combined C-H functionalization/cope rearrangement with vinyl ethers as a surrogate for the vinylogous Mukaiyama aldol reaction

Lian, Yajing,Davies, Huw M. L.

supporting information; experimental part, p. 11940 - 11943 (2011/09/21)

Vinyl ethers selectively undergo the combined C-H functionalization/Cope rearrangement reaction via an s-cis/boat transition state. With chiral dirhodium catalysts, products are generated in a highly diastereoselective and enantioselective fashion. This r

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