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Methyl [(4-nitrophenyl)sulphonyl]carbamate, also known as aldicarb, is a chemical compound with the formula C7H6N2O4S. It is a white crystalline solid that is used as an insecticide and acaricide. Aldicarb is a carbamate pesticide, which means it works by inhibiting the acetylcholinesterase enzyme in the nervous system of insects, leading to their paralysis and death. It is highly effective against a wide range of pests, including aphids, mites, and soil-dwelling insects. However, due to its high toxicity to humans and potential to contaminate groundwater, its use has been restricted or banned in many countries. Aldicarb is also known for its rapid degradation in the environment, which can reduce its persistence in soil and water.

3337-70-0

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3337-70-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3337-70-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,3 and 7 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3337-70:
(6*3)+(5*3)+(4*3)+(3*7)+(2*7)+(1*0)=80
80 % 10 = 0
So 3337-70-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H8N2O6S/c1-16-8(11)9-17(14,15)7-4-2-6(3-5-7)10(12)13/h2-5H,1H3,(H,9,11)

3337-70-0SDS

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 methyl N-(4-nitrophenyl)sulfonylcarbamate

1.2 Other means of identification

Product number -
Other names methyl N-nosylcarbamate

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:3337-70-0 SDS

3337-70-0Relevant academic research and scientific papers

Rapid and straightforward transesterification of sulfonyl carbamates

Isaksson, Rebecka,Kumpi?a, Ilze,Larhed, Mats,Wannberg, Johan

supporting information, p. 1476 - 1478 (2016/03/12)

A fast and convenient method for the alkoxy exchange of sulfonyl carbamates by simply heating in a chosen alkyl alcohol is described. No catalysts or additives are required. Microwave heating at 100-120 °C for 20-60 min resulted in good to excellent yields (53-93%) of alkyl (arylsulfonyl)carbamates where the alkyl part originates from the alcohol solvent. The developed protocol was applied to the synthesis of an angiotensin II type 2 receptor (AT2R) ligand.

A catalytic, Bronsted base strategy for intermolecular allylic C-H amination

Reed, Sean A.,Mazzotti, Anthony R.,White, M. Christina

supporting information; experimental part, p. 11701 - 11706 (2009/12/08)

A Bronsted base activation mode for oxidative, Pd(II)/sulfoxide- catalyzed, intermolecular C-H allylic amination is reported. N,N-diisopropylethylamine was found to promote amination of unactivated terminal olefins, forming the corresponding linear allylic amine products with high levels of stereo-, regio-, and chemoselectivity. The predictable and high selectivity of this C-H oxidation method enables latestage incorporation of nitrogen into advanced synthetic intermediates and natural products.

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