Cas 1613380-61-2,(2R,3R)-ethyl 3-(4-chlorophenyl)-2-(diethoxyphosphoryl)-2-fluoropent-4-enoate

1613380-61-2

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Basic information

Product Name: (2R,3R)-ethyl 3-(4-chlorophenyl)-2-(diethoxyphosphoryl)-2-fluoropent-4-enoate
Synonyms: (2R,3R)-ethyl 3-(4-chlorophenyl)-2-(diethoxyphosphoryl)-2-fluoropent-4-enoate
CAS NO:1613380-61-2
Molecular Formula:
Molecular Weight: 392.792
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: (2R,3R)-ethyl 3-(4-chlorophenyl)-2-(diethoxyphosphoryl)-2-fluoropent-4-enoate(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3R)-ethyl 3-(4-chlorophenyl)-2-(diethoxyphosphoryl)-2-fluoropent-4-enoate(1613380-61-2)
EPA Substance Registry System: (2R,3R)-ethyl 3-(4-chlorophenyl)-2-(diethoxyphosphoryl)-2-fluoropent-4-enoate(1613380-61-2)

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: 1613380-61-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1613380-61-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,3,3,8 and 0 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1613380-61:
(9*1)+(8*6)+(7*1)+(6*3)+(5*3)+(4*8)+(3*0)+(2*6)+(1*1)=142
142 % 10 = 2
So 1613380-61-2 is a valid CAS Registry Number.

1613380-61-2Upstream product

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1613380-61-2Relevant academic research and scientific papers

Pd-catalyzed highly regio-, diastereo-, and enantioselective allylic alkylation of α-fluorophosphonates

Huang, Ying,Zhang, Qing-Song,Fang, Ping,Chen, Tie-Gen,Zhu, Jun,Hou, Xue-Long

, p. 6751 - 6753 (2014)

Highly efficient Pd-catalyzed asymmetric allylic alkylation reaction of ethyl-2-fluoro-2-(diethoxyphosphoryl)acetate with monosubstituted allylic substrates has been developed, affording corresponding α- fluorophosphonates with two chiral centers in high

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