75937-17-6

Basic information

• Product Name: Carbamic acid, [2-[(2-hydroxyethyl)thio]ethyl]-, 1,1-dimethylethyl ester
• CAS NO: 75937-17-6
• Molecular Formula: C9H19NO3S
• Molecular Weight: 221.31700
• Mol File: 75937-17-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Carbamic acid, [2-[(2-hydroxyethyl)thio]ethyl]-, 1,1-dimethylethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, [2-[(2-hydroxyethyl)thio]ethyl]-, 1,1-dimethylethyl ester(75937-17-6)
• EPA Substance Registry System: Carbamic acid, [2-[(2-hydroxyethyl)thio]ethyl]-, 1,1-dimethylethyl ester(75937-17-6)

Safety Data

• Hazardous Substances Data: 75937-17-6(Hazardous Substances Data)

Usage

General Description

The chemical compound Carbamic acid, [2-[(2-hydroxyethyl)thio]ethyl]-, 1,1-dimethylethyl ester, also known as thiodicarb, is a carbamate insecticide and acaricide. It is commonly used to control a wide range of pests, including aphids, caterpillars, mites, and whiteflies, on various crops such as vegetables, fruits, and ornamentals. Thiodicarb works by inhibiting the activity of acetylcholinesterase, an enzyme essential for the proper functioning of the nervous system in insects. This disrupts their neurotransmission and ultimately leads to paralysis and death. However, thiodicarb is also known to be toxic to beneficial insects, so its use should be carefully controlled to minimize negative impacts on non-target species and the environment.

Upstream product

• 67385-10-8 di-tert-butyl(disulfanediylbis(ethane-2,1-diyl))dicarbamate 
• 24304-84-5 2-[(2-aminoethyl)thio]ethanol 
• 24424-99-5 di-tert-butyl dicarbonate 
• 39684-80-5 2-(tert-butoxycarbonylamino)ethyl bromide 
• 60-24-2 2-hydroxyethanethiol 
• 26690-80-2 2-(N-tert-butoxycarbonylamino)ethanol 
• 67385-09-5 2-[(tert-butoxycarbonyl)amino]-1-ethanethiol 
• 540-51-2 2-bromoethanol 
• 107-07-3 2-chloro-ethanol 
• 158690-56-3 2-(tert-butoxycarbonylamino)ethyl-4-methylbenzenesulfonate 

Downstream Products

• 142604-13-5 2-<<(N-t-Boc)-2-aminoethyl>sulphonyl>ethanol 

Relevant articles and documents

ADHESIVE PHOTOPROTECTIVE COMPOUNDS AND USES THEREOF

The present invention relates to a compound represented by the following formula (I): A[B-(C)v]w, wherein A is a photoprotective moiety, B is a linker, C is a functional group, v is an integer from 1 to 2000, and w is an integer from

FUSED HETEROCYCLIC COMPOUND

A compound of the formula: wherein ring'' A is a 7-membered or 8-membered nitrogen- containing ring optionally further substituted, ring B is an optionally substituted aryl group or an optionally substituted heteroaryl group, X1 is a group represented by -NR3-Y1-, -0-, -S-, -SO-, -SO2- or -CHR3- wherein R3 is a hydrogen atom or'' an optionally substituted aliphatic hydrocarbon group, or R3 may be bonded to the carbon atom of ring B to form an optionally substituted ring structure, and Y1 is a bond or an optionally substituted C1-4 alkylene, R1 is a hydrogen atom, or an optionally substituted group bonded via a carbon atom or a sulfur atom, the formula = shows a single bond or a double bond, when ===R2 is - R2, R2 is a hydrogen atom, or an optionally substituted group bonded via a carbon atom, a nitrogen atom, an oxygen atom or a sulfur atom, and when ===R2 is =R2, R2 is an oxo group, an optionally substituted alkylidene group, or an optionally, substituted imino group.

An N-terminal method for peptide solubilisation

Peptide-constructs of the form (solubilising peptide)- [NH(CH2)2SO2(CH2)2O-CO]-(insoluble peptide) were synthesised by Boc SPPS. The HPLC-purified peptide-constructs were cleaved with aqueous base to liberate the insoluble peptides as precipitates.