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29508-16-5

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29508-16-5 Usage

General Description

Sodium (Carbomethoxy)methane Sulfonate is a chemical compound that is mainly used in the industry as an intermediate for the production of other chemicals or as a reagent in a variety of chemical reactions. It is characterized by its solubility in water and its crystalline or powder form. The compound is typically stable in normal temperatures and pressures, but it may pose risks on human health upon prolonged exposure or ingestion. As such, proper handling and storage are crucial when using this compound. As a sulfonate, it can also serve as a surfactant, enhancing the cleaning capacity of detergents, or as an emulsifying agent, promoting the mixing of substances that do not usually combine easily, like oil and water.

Check Digit Verification of cas no

The CAS Registry Mumber 29508-16-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,5,0 and 8 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 29508-16:
(7*2)+(6*9)+(5*5)+(4*0)+(3*8)+(2*1)+(1*6)=125
125 % 10 = 5
So 29508-16-5 is a valid CAS Registry Number.
InChI:InChI=1/C4H8O5S.Na/c1-2-9-4(5)3-10(6,7)8;/h2-3H2,1H3,(H,6,7,8);/q;+1/p-1/rC4H7NaO5S/c1-2-9-4(6)3-11(7,8)10-5/h2-3H2,1H3

29508-16-5SDS

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 sodium,2-methoxy-2-oxoethanesulfonate

1.2 Other means of identification

Product number -
Other names sodium methyl 2-sulfoacetate

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:29508-16-5 SDS

29508-16-5Relevant articles and documents

Clickable transformation of nitriles (RCN) to oxazolyl sulfonyl fluoride warheads

Fang, Wan-Yin,Wang, Shi-Meng,Zhang, Zai-Wei,Qin, Hua-Li

supporting information, p. 8904 - 8909 (2020/11/30)

The protocol for simple, efficient, and mild synthesis of oxazolyl sulfonyl fluorides was developed through Rh2(OAc)4-catalyzed annulation of methyl-2-diazo-2-(fluorosulfonyl)acetate (MDF) or its ethyl ester derivative with nitriles. This practical method provides a general and direct route to a unique class of highly functionalized oxazolyl-decorated sulfonyl fluoride warheads with great potential in medicinal chemistry, chemical biology, and drug discovery.

A Knoevenagel type synthesis of styrene ω sulfinanilides

Oliver,DeMilo

, p. 321 - 322 (2007/10/10)

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