Cas 1315576-01-2,(3S,4S)-tert-butyl 4-(4-chlorophenyl)-4-(diethoxyphosphoryl)-3-methylcyclopent-1-enecarboxylate

1315576-01-2

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Basic information

Product Name: (3S,4S)-tert-butyl 4-(4-chlorophenyl)-4-(diethoxyphosphoryl)-3-methylcyclopent-1-enecarboxylate
Synonyms: (3S,4S)-tert-butyl 4-(4-chlorophenyl)-4-(diethoxyphosphoryl)-3-methylcyclopent-1-enecarboxylate
CAS NO:1315576-01-2
Molecular Formula:
Molecular Weight: 428.893
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: (3S,4S)-tert-butyl 4-(4-chlorophenyl)-4-(diethoxyphosphoryl)-3-methylcyclopent-1-enecarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (3S,4S)-tert-butyl 4-(4-chlorophenyl)-4-(diethoxyphosphoryl)-3-methylcyclopent-1-enecarboxylate(1315576-01-2)
EPA Substance Registry System: (3S,4S)-tert-butyl 4-(4-chlorophenyl)-4-(diethoxyphosphoryl)-3-methylcyclopent-1-enecarboxylate(1315576-01-2)

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: 1315576-01-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1315576-01-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,5,5,7 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1315576-01:
(9*1)+(8*3)+(7*1)+(6*5)+(5*5)+(4*7)+(3*6)+(2*0)+(1*1)=142
142 % 10 = 2
So 1315576-01-2 is a valid CAS Registry Number.

1315576-01-2Upstream product

1262883-53-3 (+/-)-tert-butyl penta-2,3-dienoate

1315576-01-2Downstream Products

1315576-01-2Relevant academic research and scientific papers

Application of a new chiral phosphepine to the catalytic asymmetric synthesis of highly functionalized cyclopentenes that bear an array of heteroatom-substituted quaternary stereocenters

Fujiwara, Yuji,Fu, Gregory C.

supporting information; experimental part, p. 12293 - 12297 (2011/10/02)

Through the design and synthesis of a new chiral phosphepine, the first catalytic asymmetric method for the [3 + 2] cycloaddition of allenes with olefins has been developed that generates cyclopentenes that bear nitrogen-, phosphorus-, oxygen-, and sulfur

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