2104-00-9

Basic information

• Product Name: LABOTEST-BB LT01281636
• Synonyms: SALOR-INT L481394-1EA;LABOTEST-BB LT01281636;4-(4-CHLOROPHENYL)-1,3-THIAZOLE-2-THIOL;4-(4-Chlorophenyl)-4-thiazoline-2-thione;2-thiazolethiol, 4-(4-chlorophenyl)-;4-(4-chlorophenyl)-3H-1,3-thiazole-2-thione;4-(4-chlorophenyl)-3H-thiazole-2-thione;4-(4-Chloro-phenyl)-thiazole-2-thiol
• CAS NO: 2104-00-9
• Molecular Formula: C₉H₆ClNS₂
• Molecular Weight: 227.73
• Mol File: 2104-00-9.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 359.3 °C at 760 mmHg
• Flash Point: 171.1 °C
• Appearance: /
• Density: 1.49
• CAS DataBase Reference: LABOTEST-BB LT01281636(CAS DataBase Reference)
• NIST Chemistry Reference: LABOTEST-BB LT01281636(2104-00-9)
• EPA Substance Registry System: LABOTEST-BB LT01281636(2104-00-9)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 2104-00-9(Hazardous Substances Data)

Usage

General Description

LABOTEST-BB LT01281636 is a chemical compound with the molecular formula C20H36O2, commonly known as dodecyl acetate. It is a derivative of acetic acid and is widely used in the cosmetic and fragrance industry as a conditioning agent and emollient. Dodecyl acetate is a clear, colorless liquid with a mild, pleasant odor and is known for its moisturizing and lubricating properties, making it a popular ingredient in lotions, creams, and hair care products. Additionally, it is also used as a fragrance ingredient in perfumes and other scented products. Overall, LABOTEST-BB LT01281636 is a versatile chemical with various applications in the beauty and personal care industry.

Upstream product

• 507-09-5 thioacetic acid 
• 19339-59-4 1-(4-chloro-phenyl)-2-thiocyanato-ethanone 
• 22535-06-4 p-chloro-phenacyl bromide 
• 54608-14-9 ammonium dithiocarbonate 
• 94210-44-3 2,2'-bis[4-(p-chlorophenyl)thiazyl]disulfide 
• 25917-49-1 1-(4-chlorophenyl)-2-(p-tolylsulfonyloxy)ethanone 
• 513-74-6 ammonium dithiocarbamate 
• 352200-57-8 N-(5-methyl-1-phenyl-4-hexen-1-oxy)-4-(p-chlorophenyl)-thiazole-2(3H)-thione 
• 333-20-0 potassium thioacyanate 
• 99-91-2 para-chloroacetophenone 
• 17356-08-0 thiourea 
• 123466-28-4 [(4-chlorophenyl)ethynyl](phenyl)iodonium tosylate 
• 536-38-9 4-chlorobenzoylmethyl bromide 

Downstream Products

• 69390-12-1 2-butylsulfanyl-4-(4-chloro-phenyl)-thiazole 
• 2103-97-1 4-(4-chlorophenyl)-2-(methylthio)thiazole 
• 97833-30-2 4-(4-chloro-phenyl)-2-phenyldisulfanyl-thiazole 
• 97284-40-7 4-(4-chloro-phenyl)-2-(4-chloro-phenyldisulfanyl)-thiazole 
• 105469-45-2 3a,3b-Bis-(4-chloro-phenyl)-hexahydro-1,6-dithia-3,4-diaza-cyclobutadicyclopentene-2,5-dithione 
• 130459-60-8 [4-(4-Chloro-phenyl)-thiazol-2-ylsulfanyl]-acetonitrile 
• 1036227-66-3 [4-(4-chloro-phenyl)-thiazol-2-ylsulfanyl]-acetic acid tert-butyl ester 
• 130459-70-0 3-[4-(4-Chloro-phenyl)-thiazol-2-ylsulfanyl]-chromen-2-one 
• 130459-64-2 3-[4-(4-Chloro-phenyl)-thiazol-2-ylsulfanyl]-chromen-2-ylideneamine 
• 130459-68-6 3-[4-(4-Chloro-phenyl)-thiazol-2-ylsulfanyl]-8-methoxy-chromen-2-ylideneamine 
• 130459-72-2 3-[4-(4-Chloro-phenyl)-thiazol-2-ylsulfanyl]-8-methoxy-chromen-2-one 
• 97284-39-4 4-(4-chloro-phenyl)-2-(2-chloro-phenyldisulfanyl)-thiazole 
• 97319-78-3 2-(4-chloro-2-nitro-phenyldisulfanyl)-4-(4-chloro-phenyl)-thiazole 

Relevant articles and documents

Synthesis of novel azabicyclo derivatives containing a thiazole moiety and their biological activity against pine-wood nematodes

To explore a new skeleton with nematicidal activity, a series of novel azabicyclo derivatives containing a thiazole moiety were designed, synthesized and evaluated for their nematicidal activities. The bioassay results against pine-wood nematodes (Bursaphelenchus xylophilus) showed that most of the title compounds displayed nematicidal activity at a concentration of 40 mg/L. Especially, the title compounds2-((8-methyl-8-azabicyclo[3.2.1]octan-3-yl)oxy)-4-(4-chlorophenyl)thiazole (7e), 2-((8-methyl-8-azabicyclo[3.2.1]octan-3-yl)thio)-4-phenylthiazole (10a) and 2-((8-methyl-8-azabicyclo [3.2.1]octan-3-yl)thio)-4-(4-chlorophenyl)thiazole (10e) exhibited more than 90% mortality against Bursaphelenchus xylophilus.

2-[3H-THIAZOL-2-YLIDINEMETHYL]PYRIDINES AND RELATED COMPOUNDS AND THEIR USE

The present invention pertains to certain 2-[3H-thiazol-2-ylidinemethyl]pyridine compounds and analogs thereof, which, inter alia, inhibit cell proliferation, treat cancer, etc., and more specifically to compounds of the following formula, wherein RA1, RA2, RA3, RA4, RB1, RB2, RNA, RNB, and X? are as defined herein: The present invention also pertains to pharmaceutical compositions comprising such compounds, and the use of such compounds and compositions, both in vitro and in vivo, to inhibit cell proliferation, and in the treatment of proliferative conditions such as cancer, etc.

Synthesis and evaluation of some substituted mercaptothiazoles and their derivatives of biological interest

The title compounds have been synthesized from 4-(4′ -chlorophenyl)-Δ4-thiazoline-2-thione1, which in turn is synthesized by the reaction of p-chlorophenacyl bromide with ammonium dithiocarbamate. Compound 1 on treatment with N-chlor