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Phosphonic acid, (3-chloro-2-hydroxypropyl)-, diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65345-16-6

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65345-16-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65345-16-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,3,4 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 65345-16:
(7*6)+(6*5)+(5*3)+(4*4)+(3*5)+(2*1)+(1*6)=126
126 % 10 = 6
So 65345-16-6 is a valid CAS Registry Number.

65345-16-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloro-3-diethoxyphosphorylpropan-2-ol

1.2 Other means of identification

Product number -
Other names (+/-)-diethyl 3-chloro-2-hydroxypropanephosphonate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:65345-16-6 SDS

65345-16-6Downstream Products

65345-16-6Relevant academic research and scientific papers

A novel synthesis of diethyl (R)-3-(N-benzyloxyamino)-2- hydroxypropylphosphonate, a precursor to hydroxylamine antibiotics FR-33289 and FR-33699

Wroblewski, Andrzej E.,Halajewska-Wosik, Anetta

, p. 3201 - 3205 (2007/10/03)

Regioselective opening of the oxirane ring at C(3) of diethyl 2,3-epoxypropylphosphonate 6 with N- or O-benzylhydroxylamine led to 3-(N-benzyl-N-hydroxyamino)- or 3-(N-benzyloxyamino)-2- hydroxypropylphosphonates, 10 or 8. From (S)-6 (ee 94%), the phosphonate (S)-10 (ee 98%) was prepared in 80% yield. Highly enantiomerically enriched (R)- and (S)-8 (ee 97%) were obtained from (R)- and (S)-6 (ee 88% and 94%), respectively.

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