METHYL THIOSALICYLATE

METHYL THIOSALICYLATE Basic information
Product Name:METHYL THIOSALICYLATE
Synonyms:METHYL THIOSALICYLAT;Methyl 2-Thiosalicylate;NSC 30156;o-Mercapto-benzoic Acid Methyl Ester;Thiosalicylic Acid Methyl Ester Methyl 2-Mercaptobenzoate 2-Mercaptobenzoic Acid Methyl Ester;2-Mercaptobenzoic acid methyl;Methyl thiosalicylate,97%;Methylethiosalicylate, 97%
CAS:4892-02-8
MF:C8H8O2S
MW:168.21
EINECS:628-716-4
Product Categories:fine chemicals;Organics;Metal Isotopes;Sulfur & Selenium Compounds
Mol File:4892-02-8.mol
METHYL THIOSALICYLATE Structure
METHYL THIOSALICYLATE Chemical Properties
Melting point 164 °C
Boiling point 98-100 °C/2 mmHg (lit.)
density 1.223 g/mL at 25 °C (lit.)
refractive index n20/D 1.591(lit.)
Fp >230 °F
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
pka5.84±0.43(Predicted)
form Liquid
Specific Gravity1.223
color Clear colorless to light yellow or light green
Sensitive Air Sensitive
Stability:Air Sensitive
CAS DataBase Reference4892-02-8(CAS DataBase Reference)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 20/21/22-36/37/38
Safety Statements 26-37/39
WGK Germany 3
RTECS DH3500000
HazardClass IRRITANT
HS Code 29309090
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
METHYL THIOSALICYLATE Usage And Synthesis
Chemical Propertiesclear colorless to light yellow or light green
UsesMethyl thiosalicylate may be used:
  • in the synthesis of thioxanthone, an efficient enantioselective organocatalyst for the intramolecular [2+2] photocycloaddition reaction
  • as anionic bidentate ligand, in the preparation of ′2+1′ type complexes of [(99m)Tc]-tricarbonyltechnetium(I) and [(188)Re]-tricarbonylrhenium(I)
  • in the synthesis of a series of benzisothiazolone derivatives
  • in the synthesis of a new fused benzoheterocyclic compound, [1]benzothieno[3,2-b]furan
UsesMethyl 2-Mercaptobenzoate (cas# 4892-02-8) is a compound useful in organic synthesis.
General DescriptionMethyl thiosalicylate may be benefecial in preventing mercury-induced toxicity.
METHYL THIOSALICYLATE Preparation Products And Raw materials
Preparation Products2-MERCAPTOBENZYL ALCOHOL-->METHYL 3-HYDROXYBENZO[B]THIOPHENE-2-CARBOXYLATE
dimethyl 2,2'-dithiobisbenzoate METHYL 2-[(CYANOMETHYL)THIO]BENZOATE DPX-T5648 METHYL 2-[(CYANOMETHYL)SULFONYL]BENZOATE METHYL 2-[(5-FORMYLIMIDAZO[2,1-B][1,3]THIAZOL-6-YL)SULFANYL]BENZENECARBOXYLATE METHYL 2-[(5-NITROIMIDAZO[2,1-B][1,3]THIAZOL-6-YL)SULFANYL]BENZENECARBOXYLATE METHYL 2-[(5-CYANOIMIDAZO[2,1-B][1,3]THIAZOL-6-YL)SULFANYL]BENZENECARBOXYLATE METHYL 2-(METHYLTHIO)BENZOATE METHYL 2-([5-(([(2,4-DICHLOROBENZYL)OXY]IMINO)METHYL)IMIDAZO[2,1-B][1,3]THIAZOL-6-YL]SULFANYL)BENZENECARBOXYLATE Chlorimuron-ethyl METHYL 2-(2-QUINOXALINYLSULFONYL)BENZENECARBOXYLATE METHYL THIOSALICYLATE METHYL 2-((5-[(HYDROXYIMINO)METHYL]IMIDAZO[2,1-B][1,3]THIAZOL-6-YL)SULFANYL)BENZENECARBOXYLATE METHYL 2-(METHYLTHIO)-5-NITROBENZOATE 5-[(2-METHOXYCARBONYL)PHENYLTHIO]-1-METHYL-3-(TRIFLUOROMETHYLPYRAZOLE)-4-CARBOXALDEHYDE METHYL 2-(2-QUINOXALINYLSULFANYL)BENZENECARBOXYLATE METHYL 2-((5-[(METHOXYIMINO)METHYL]IMIDAZO[2,1-B][1,3]THIAZOL-6-YL)SULFANYL)BENZENECARBOXYLATE Methyl 2-(chlorosulfonyl)benzoate

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