Cas 185958-30-9,((1S,2S)-1-Hydroxy-2-phenyl-2-triisopropylsilanyloxy-ethyl)-phosphonic acid diethyl ester

185958-30-9

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Basic information

Product Name: ((1S,2S)-1-Hydroxy-2-phenyl-2-triisopropylsilanyloxy-ethyl)-phosphonic acid diethyl ester
Synonyms:
CAS NO:185958-30-9
Molecular Formula:
Molecular Weight: 430.597
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: ((1S,2S)-1-Hydroxy-2-phenyl-2-triisopropylsilanyloxy-ethyl)-phosphonic acid diethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: ((1S,2S)-1-Hydroxy-2-phenyl-2-triisopropylsilanyloxy-ethyl)-phosphonic acid diethyl ester(185958-30-9)
EPA Substance Registry System: ((1S,2S)-1-Hydroxy-2-phenyl-2-triisopropylsilanyloxy-ethyl)-phosphonic acid diethyl ester(185958-30-9)

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: 185958-30-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 185958-30-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,9,5 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 185958-30:
(8*1)+(7*8)+(6*5)+(5*9)+(4*5)+(3*8)+(2*3)+(1*0)=189
189 % 10 = 9
So 185958-30-9 is a valid CAS Registry Number.

185958-30-9Upstream product

13716-45-5 diethyl trimethylsilyl phosphite

185958-30-9Downstream Products

185958-30-9Relevant academic research and scientific papers

Stereochemical aspects of the asymmetric synthesis of chiral α,β-dihydroxy phosphonates. Synthesis of α,β-dihydroxy phosphonic acids

Bongini, Alessandro,Camerini, Roberto,Panunzio, Mauro,Bandini, Elisa,Martelli, Giorgio,Spunta, Giuseppe

, p. 3485 - 3504 (2007/10/03)

Stereocontrol in the asymmetric phosphonylation of aldehydes via organophosphorous esters has been obtained starting from chiral aldehydes. The nature of the O-protecting group is crucial to obtain, in terms of diastereoselectivity and chemical yields, th

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