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62327-21-3

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62327-21-3 Usage

Description

tert-Butyl O,O-dimethylphosphonoacetate is an organic compound that serves as a versatile reagent and intermediate in the synthesis of various chemical compounds and pharmaceuticals. It is characterized by its phosphonoacetate group, which is a key functional group in many biologically active molecules.

Uses

Used in Pharmaceutical Industry:
tert-Butyl O,O-dimethylphosphonoacetate is used as a reactant for the preparation of phosphonate terminated PPH dendrimers, which have potential applications as anti-HIV-1 agents. These dendrimers can help inhibit the replication of the HIV-1 virus, offering a promising approach to combat the disease.
Used in Organic Synthesis:
tert-Butyl O,O-dimethylphosphonoacetate is used as a reactant for the preparation of monodehydro diketopiperazines from ketoacyl amino acid amides via acid-catalyzed cyclization. This reaction is an important step in the synthesis of various natural products and pharmaceuticals.
Used in Organic Chemistry:
tert-Butyl O,O-dimethylphosphonoacetate is used as a reactant for the preparation of α,β-unsaturated esters, which are useful in the guanidine-catalyzed oxa-Michael addition. This reaction is a key step in the synthesis of various complex organic molecules.
Used in Antibacterial Agents:
tert-Butyl O,O-dimethylphosphonoacetate is used as a reactant for the preparation of myxopyronin B and desmethyl myxopyronin B analogs, which exhibit antibacterial activity and inhibitory activity against bacterial RNA polymerase. These compounds can be used as potential antibacterial agents in the development of new antibiotics.
Used in Organic Reactions:
tert-Butyl O,O-dimethylphosphonoacetate is used as a reactant in allylation and subsequent ring-closing metathesis in the presence of Grubbs' catalyst or intramolecular rhodium-catalyzed cyclopropanation reactions. These reactions are important for the synthesis of various complex organic molecules and pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 62327-21-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,3,2 and 7 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 62327-21:
(7*6)+(6*2)+(5*3)+(4*2)+(3*7)+(2*2)+(1*1)=103
103 % 10 = 3
So 62327-21-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H17O5P/c1-8(2,3)13-7(9)6-14(10,11-4)12-5/h6H2,1-5H3

62327-21-3 Well-known Company Product Price

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  • TCI America

  • (B5094)  tert-Butyl Dimethylphosphonoacetate  >95.0%(GC)

  • 62327-21-3

  • 5g

  • 390.00CNY

  • Detail
  • TCI America

  • (B5094)  tert-Butyl Dimethylphosphonoacetate  >95.0%(GC)

  • 62327-21-3

  • 25g

  • 1,290.00CNY

  • Detail
  • Aldrich

  • (79522)  tert-ButylP,P-dimethylphosphonoacetate  ≥97.0% (GC)

  • 62327-21-3

  • 79522-25ML

  • 3,967.47CNY

  • Detail
  • Aldrich

  • (79522)  tert-ButylP,P-dimethylphosphonoacetate  ≥97.0% (GC)

  • 62327-21-3

  • 79522-100ML

  • 12,296.70CNY

  • Detail

62327-21-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-Butyl P,P-dimethylphosphonoacetate

1.2 Other means of identification

Product number -
Other names tert-butyl 2-dimethoxyphosphorylacetate

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:62327-21-3 SDS

62327-21-3Relevant articles and documents

CARBAMOYL COMPOUNDS AS DGAT1 INHIBITORS 190

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Page/Page column 29; 161-162, (2009/07/25)

DGAT-1 inhibitor compounds of formula (I), pharmaceutically-acceptable salts and pro- drugs thereof are described, together with pharmaceutical compositions, processes for making them and their use in treating, for example, obesity wherein, for example, Ring A is optionally substituted 2,6-pyrazindiyl; X is =O; Ring B is optionally substituted 1,4-phenylene; Y1 is a direct bond or -O-; Y2 is -(CH 2) r- wherein r is 2 or 3; n is 0 or n is 1 when Y1 is a direct bond between Ring B and Ring C and when Ring B is 1,4-phenylene and Ring C is (4-6C)cycloalkane; Ring C is optionally substituted (4-6C)cycloalkane, (7-10C)bicycloalkane, (8-12C)tricycloalkane, phenylene or pryidindiyl; L is a direct bond or -O-; p is 0, 1 or 2 and when p is 1 or 2 RA1 and RA2 are each independently hydrogen or (1-4C)alkyl; Z is carboxy or a mimic or bioisostere thereof.

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