Cas 161912-06-7,(4-Benzyloxycarbonylmethyl-2,2,2-trichloro-5-oxo-2λ<sup>5</sup>-[1,3,2]dioxaphospholan-4-yl)-acetic acid benzyl ester

161912-06-7

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Basic information

Product Name: (4-Benzyloxycarbonylmethyl-2,2,2-trichloro-5-oxo-2λ⁵-[1,3,2]dioxaphospholan-4-yl)-acetic acid benzyl ester
Synonyms:
CAS NO:161912-06-7
Molecular Formula:
Molecular Weight: 507.691
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: (4-Benzyloxycarbonylmethyl-2,2,2-trichloro-5-oxo-2λ⁵-[1,3,2]dioxaphospholan-4-yl)-acetic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (4-Benzyloxycarbonylmethyl-2,2,2-trichloro-5-oxo-2λ⁵-[1,3,2]dioxaphospholan-4-yl)-acetic acid benzyl ester(161912-06-7)
EPA Substance Registry System: (4-Benzyloxycarbonylmethyl-2,2,2-trichloro-5-oxo-2λ⁵-[1,3,2]dioxaphospholan-4-yl)-acetic acid benzyl ester(161912-06-7)

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: 161912-06-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 161912-06-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,9,1 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 161912-06:
(8*1)+(7*6)+(6*1)+(5*9)+(4*1)+(3*2)+(2*0)+(1*6)=117
117 % 10 = 7
So 161912-06-7 is a valid CAS Registry Number.

161912-06-7Upstream product

631-25-4 tribenzyl citrate

161912-06-7Downstream Products

161912-06-7Relevant academic research and scientific papers

Synthesis via a cyclic dioxatrichlorophosphorane of 1,3-dibenzyl-2-phosphonooxy citrate

Pankowski, Andrew H.,Meehan, John D.,Sallis, John D.

, p. 927 - 930 (1994)

Phosphorylation of tribenzyl citrate with PCl5 proceeds via a cyclic dioxatrichlorophosphorane and results in the formation of 1,3-dibenzyl-2-phosphonooxy citrate. A mechanism for the phosphorylation and ester hydrolysis is proposed and the use

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