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Hydroxymethanesulfonic acid sodium salt, also known as sodium formaldehyde sulfoxylate or sodium hydroxymethylsulfinate, is a chemical compound with the formula CH3NaO2S. It is a white crystalline solid that is soluble in water and is commonly used as a reducing agent in various chemical reactions. hydroxymethanesulfonic acid sodium salt is particularly effective in the reduction of nitro groups to amines, making it a valuable reagent in the synthesis of pharmaceuticals, dyes, and other organic compounds. It is also used as a preservative and disinfectant due to its ability to release formaldehyde in aqueous solutions. The compound is produced by the reaction of formaldehyde with sodium bisulfite and is considered a safer alternative to other reducing agents like sodium borohydride or sodium dithionite due to its lower toxicity and environmental impact.

820-72-4

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820-72-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 820-72-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,2 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 820-72:
(5*8)+(4*2)+(3*0)+(2*7)+(1*2)=64
64 % 10 = 4
So 820-72-4 is a valid CAS Registry Number.

820-72-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Tetrafluordimethyldiselenid

1.2 Other means of identification

Product number -
Other names -

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:820-72-4 SDS

820-72-4Downstream Products

820-72-4Relevant academic research and scientific papers

Copper-catalysed direct difluoromethylselenolation of aryl boronic acids with Se-(difluoromethyl) 4-methylbenzenesulfonoselenoate

Lu, Kui,Xi, Xiaolan,Zhou, Ting,Lei, Lingyu,Li, Quan,Zhao, Xia

, (2021)

In this study, we developed the first copper-catalysed direct difluoromethylselenolation of aryl boronic acids using Se-(difluoromethyl) 4-methylbenzenesulfonoselenoate as a difluoromethylselenolation reagent. Owing to the cheap and readily accessible reagents, broad substrate scope, and mild reaction conditions, this is an alternative and practical strategy for the synthesis of aryl difluoromethylselenylether.

Metal-Free Difluoromethylselenolation of Arylamines under Visible-Light Photocatalysis

Lu, Kui,Li, Quan,Xi, Xiaolan,Zhou, Ting,Zhao, Xia

supporting information, p. 1224 - 1231 (2020/01/02)

A novel visible-light photocatalytic difluoromethylselenolation of aryl amines via in situ generation of aryldiazonium salts was achieved using Se-(difluoromethyl) 4-methylbenzenesulfonoselenoate, which was synthesized for the first time. The reagent is readily accessible and shelf-stable. The metal-free reaction conditions and the broad substrate scope provide a green protocol for the efficient and rapid introduction of the difluoromethylselenylether group.

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