3001-64-7

Usage

Uses

Used in Pharmaceutical Industry:
2-Mercaptopropanol is used as a solvent and in the production of pharmaceuticals for its ability to dissolve a wide range of substances and facilitate chemical reactions necessary for drug synthesis.
Used in Cosmetics and Personal Care Industry:
2-Mercaptopropanol is used as a fragrance and skin conditioning agent in cosmetics and personal care products, enhancing the sensory experience and providing skin benefits.
Used in Chemical Synthesis:
2-Mercaptopropanol is used as an intermediate in the synthesis of various chemicals, including agrochemicals and rubber chemicals, contributing to the development of these industries.
Used in Metal Salt Production:
2-Mercaptopropanol is used in the production of metal salts, which are then utilized in the manufacturing of catalysts and pigments, playing a crucial role in the chemical and materials science sectors.

InChI:InChI=1/C3H8OS/c1-3(5)2-4/h3-5H,2H2,1H3

Upstream product

• 107-19-7 propargyl alcohol 
• 6405-82-9 acetyl-chloro-sulfane 
• 292638-85-8 acrylic acid methyl ester 
• 79-42-5 2-mercaptopropanoic acid 
• 73232-07-2 2-ethoxythiocarbonyl sulfanyl-propionic acid ethyl ester 
• 53907-46-3 methyl 2-mercaptopropionate 

Downstream Products

• 72311-96-7 2-ethylthio-2-propanol 
• 1072-43-1 propylene sulphide 
• 20463-93-8 2-(methylthio)-2-methylethanol 
• 32300-62-2 2-(2,4-dinitro-phenylsulfanyl)-propan-1-ol 

Relevant academic research and scientific papers

PBD CONJUGATES FOR TREATING DISEASES

The present disclosure relates to pyrrolobenzodiazepine (PBD) prodrugs and conjugates thereof. The present disclosure also relates to pharmaceutical compositions of the conjugates described herein, methods of making and methods of using the same.

AMINO-QUINOLINES AS KINASE INHIBITORS

Disclosed are quinoline compounds having the formula: wherein R1, R2 and A are as defined herein, and methods of making and using the same.

1-(CHLOROMETHYL)-2,3-DIHYDRO-1H-BENZO[E]INDOLE DIMER ANTIBODY-DRUG CONJUGATE COMPOUNDS, AND METHODS OF USE AND TREATMENT

The invention provides antibody-drug conjugates comprising an antibody conjugated to a 1-(chloromethyl)-2,3-dihydro-1H-benzo[e]indole (CBI) dimer drug moiety via a linker, and methods of using the antibody-drug conjugates.

Triphendioxazine dyestuffs

The novel triphendioxazine dyestuffs of the formula STR1 in which the substituents R, R', T1, T2, X, Y and n have the meanings given in the description are highly suitable for the dyeing and printing of cellulose-containing or amido-containing material.

Synthesis and Insecticidal Activity of Oxazaphospholidines, Oxathiaphospholanes, and Thiazaphospholidines

Fifty-five new five-membered cyclic organophosphorus compounds including oazaphospholidines, thiazaphospholidines, and oxathiaphospholanes were synthesized, which have substituents at 4- or/and 5-positions besides at the 2-position.The thiazaphospholidines showed the highest insecticidal activity followed by oxathiaphospholanes and oxazaphospholidines.The position preference of substituents in insecticidal activity was most obvious in the oxazaphospholidines.It was preferable for insecticidal activity to have the substituent near the more basic atom: the 4-position for thiazaphospholidine and oxazaphospholidine, the 5-position for oxathiaphospholane, with the exception of 4- or 5-phenyl oxazaphospholidine.

THE CHEMISTRY OF α,ω-MERCAPTOALCOHOLS IN THE PRESENCE OF DIETHOXYTRIPHENYLPHOSPHORANE. TEMEPERATURE DEPENDENCE OF CYCLODEHYDRATIONS AND S-ETHYLATIONS

Diethoxytriphenylphosphorane (DTPP) is easily prepared by oxidative addition of triphenylphosphine with diethyl peroxide.DTPP converts a variety of mercaptoalcohols to cyclic sulfides as well as hydroxythioethers.The temperature dependence (+25 --> -25 deg C) of the product distribution has synthetic petential.