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16713-66-9

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16713-66-9 Usage

Chemical Properties

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Check Digit Verification of cas no

The CAS Registry Mumber 16713-66-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,1 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 16713-66:
(7*1)+(6*6)+(5*7)+(4*1)+(3*3)+(2*6)+(1*6)=109
109 % 10 = 9
So 16713-66-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H14O4/c10-7(11)5-9(6-8(12)13)3-1-2-4-9/h1-6H2,(H,10,11)(H,12,13)/p-2

16713-66-9 Well-known Company Product Price

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  • Alfa Aesar

  • (B20146)  3,3-Tetramethyleneglutaric acid, 98+%   

  • 16713-66-9

  • 25g

  • 524.0CNY

  • Detail
  • Alfa Aesar

  • (B20146)  3,3-Tetramethyleneglutaric acid, 98+%   

  • 16713-66-9

  • 100g

  • 1957.0CNY

  • Detail

16713-66-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Cyclopentane-1,1-diacetic acid

1.2 Other means of identification

Product number -
Other names 1,1-Cyclopentanediacetic Acid

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:16713-66-9 SDS

16713-66-9Relevant articles and documents

Antiproliferative and antibacterial activity of some glutarimide derivatives

Popovi?-Djordjevi?, Jelena B.,Klaus, Anita S.,?i?ak, ?eljko S.,Mati?, Ivana Z.,Drakuli?, Branko J.

, p. 915 - 923 (2016/10/09)

Antiproliferative and antibacterial activities of nine glutarimide derivatives (1–9) were reported. Cytotoxicity of compounds was tested toward three human cancer cell lines, HeLa, K562 and MDA-MB-453 by MTT assay. Compound 7 (2-benzyl-2-azaspiro[5.11]heptadecane-1,3,7-trione), containing 12-membered ketone ring, was found to be the most potent toward all tested cell lines (IC50 = 9–27 μM). Preliminary screening of antibacterial activity by a disk diffusion method showed that Gram-positive bacteria were more susceptible to the tested compounds than Gram-negative bacteria. Minimum inhibitory concentration (MIC) determined by a broth microdilution method confirmed that compounds 1, 2, 4, 6–8 and 9 inhibited the growth of all tested Gram-positive and some of the Gram-negative bacteria. The best antibacterial potential was achieved with compound 9 (ethyl 4-(1-benzyl-2,6-dioxopiperidin-3-yl)butanoate) against Bacillus cereus (MIC 0.625 mg/mL; 1.97 × 10?3mol/L). Distinction between more and less active/inactive compounds was assessed from the pharmacophoric patterns obtained by molecular interaction fields.

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