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64496-78-2

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64496-78-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64496-78-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,4,9 and 6 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 64496-78:
(7*6)+(6*4)+(5*4)+(4*9)+(3*6)+(2*7)+(1*8)=162
162 % 10 = 2
So 64496-78-2 is a valid CAS Registry Number.

64496-78-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name salicylic acid-(2-chloro-ethyl ester)

1.2 Other means of identification

Product number -
Other names 1-Salicyloxy-2-Cl-ethan

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:64496-78-2 SDS

64496-78-2Relevant articles and documents

Cytotoxic Activity of Salicylic Acid-Containing Drug Models with Ionic and Covalent Binding

Egorova, Ksenia S.,Seitkalieva, Marina M.,Posvyatenko, Alexandra V.,Khrustalev, Victor N.,Ananikov, Valentine P.

, p. 1099 - 1104 (2015)

Three different types of drug delivery platforms based on imidazolium ionic liquids (ILs) were synthesized in high preparative yields, namely, the models involving (i) ionic binding of drug and IL; (ii) covalent binding of drug and IL; and (iii) dual binding using both ionic and covalent approaches. Seven ionic liquids containing salicylic acid (SA-ILs) in the cation or/and in the anion were prepared, and their cytotoxicity toward the human cell lines CaCo-2 (colorectal adenocarcinoma) and 3215 LS (normal fibroblasts) was evaluated. Cytotoxicity of SA-ILs was significantly higher than that of conventional imidazolium-based ILs and was comparable to the pure salicylic acid. It is important to note that the obtained SA-ILs dissolved in water more readily than salicylic acid, suggesting benefits of possible usage of traditional nonsoluble active pharmaceutical ingredients in an ionic liquid form.

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