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15102-51-9

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15102-51-9 Usage

General Description

2-[(2,2-dichloroacetyl)amino]acetic acid is a chemical compound with the molecular formula C4H6Cl2NO3. It is a derivative of acetic acid and contains a dichloroacetyl group. 2-[(2,2-dichloroacetyl)amino]acetic acid has applications in the field of medicinal chemistry, particularly as a building block for the synthesis of pharmaceuticals and bioactive compounds. It may also be used in research and development of new drugs. Additionally, it is used in the production of other organic compounds and materials. The presence of the dichloroacetyl group makes it important to handle this chemical with care and use appropriate safety precautions. Overall, 2-[(2,2-dichloroacetyl)amino]acetic acid is a versatile compound with various potential applications in the chemical and pharmaceutical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 15102-51-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,1,0 and 2 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 15102-51:
(7*1)+(6*5)+(5*1)+(4*0)+(3*2)+(2*5)+(1*1)=59
59 % 10 = 9
So 15102-51-9 is a valid CAS Registry Number.
InChI:InChI=1/C4H5Cl2NO3/c5-3(6)4(10)7-1-2(8)9/h3H,1H2,(H,7,10)(H,8,9)

15102-51-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(2,2-dichloroacetyl)amino]acetic acid

1.2 Other means of identification

Product number -
Other names Dichloracetylglycin

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:15102-51-9 SDS

15102-51-9Relevant articles and documents

Design, synthesis, antimicrobial, and DNA gyrase inhibitory properties of fluoroquinolone–dichloroacetic acid hybrids

Seliem, Israa A.,Panda, Siva S.,Girgis, Adel S.,Nagy, Yosra I.,George, Riham F.,Fayad, Walid,Fawzy, Nehmedo G.,Ibrahim, Tarek S.,Al-Mahmoudy, Amany M. M.,Sakhuja, Rajeev,Abdel-samii, Zakaria K. M.

, p. 248 - 259 (2020)

A series of new fluoroquinolone conjugates 8a–g and 9a–f were synthesized via benzotriazole-mediated synthetic approach with good yield and purity. Some of the synthesized analogs exhibited significant antibacterial properties against Escherichia coli and

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