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7396-44-3

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7396-44-3 Usage

General Description

Diethyl (benzyloxycarbonylmethyl)phosphonate, 98% is a chemical compound with a purity of 98%. It is a phosphonate ester that is commonly used in organic synthesis as a reagent for the preparation of various organic compounds. Diethyl (benzyloxycarbonylmethyl)phosphonate, 98 % is known for its high purity and is often used in pharmaceutical and medicinal chemistry applications. It has a wide range of uses in the synthesis of complex molecules and is valued for its ability to facilitate a variety of chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 7396-44-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,9 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7396-44:
(6*7)+(5*3)+(4*9)+(3*6)+(2*4)+(1*4)=123
123 % 10 = 3
So 7396-44-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H19O5P/c1-3-17-19(15,18-4-2)11-13(14)16-10-12-8-6-5-7-9-12/h5-9H,3-4,10-11H2,1-2H3

7396-44-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl 2-diethoxyphosphorylacetate

1.2 Other means of identification

Product number -
Other names benzyl diethylphosphonoacetate

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:7396-44-3 SDS

7396-44-3Relevant articles and documents

Ir-Catalyzed Remote Functionalization by the Combination of Deconjugative Chain-Walking and C-H Activation Using a Transient Directing Group

Tang, King Hung Nigel,Uchida, Kanako,Nishihara, Kazuki,Ito, Mamoru,Shibata, Takanori

supporting information, p. 1313 - 1317 (2022/02/23)

An Ir-catalyzed reaction of N-benzylideneanilines with functionalized alkenes such as α,β-unsaturated esters gave ortho-substituted benzaldehyde derivatives with a functional group at the remote position after acidic treatment. The present transformation

Synthesis of orthogonally protected (2S)-2-amino-adipic acid (α-AAA) and (2S,4 R)-2-amino-4-hydroxyadipic acid (Ahad)

Yadav, Saroj,Taylor, Carol M.

, p. 5401 - 5409 (2013/07/26)

(2S,4R)-2-Amino-4-hydroxyadipic acid (Ahad) building block 45 was synthesized in 11 steps and 6.5% overall yield from commercially available materials. Key steps in stereocontrol were an asymmetric conjugate addition employing a proline-based catalyst and a syn-selective intramolecular-conjugate addition of an oxygen nucleophile to an α,β-unsaturated ester. To enable incorporation of α-amino-adipic acid (α-AAA) and Ahad into peptides, a truly orthogonal protecting group scheme was developed, encompassing an allyloxycarbonyl (Alloc) carbamate for Nα, a tert-butyl ester for the δ-COOH, an acetol ester for the α-COOH, and a tert- butyldimethylsilyl ether for the γ-hydroxy group of Ahad.

METHOD AND DEVICE

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Page/Page column 17-18, (2008/06/13)

A method of providing suspended cells (10) for carrying out biological assays, comprising the steps of: a) providing a frozen cell suspension, b) bringing the frozen cell suspension into direct contact with an excess volume of thawing buffer (12), and c) incubating the solution of step b) at room temperature in order to thaw the cell suspension.

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