618-03-1

Usage

Flammability and Explosibility

Notclassified

InChI:InChI=1/C7H9NO3S/c1-5-2-3-6(4-7(5)8)12(9,10)11/h2-4H,8H2,1H3,(H,9,10,11)

Upstream product

• 36717-39-2 2,2'-dimethyldianilinium sulfate 
• 7664-93-9 sulfuric acid 
• 95-53-4 o-toluidine 
• 88-72-2 1-methyl-2-nitrobenzene 
• 104-15-4 toluene-4-sulfonic acid 
• 97-06-3 4-methyl-3-nitro-benzenesulfonic acid 

Downstream Products

• 4592-97-6 2,3,5-trichloro-6-methyl-1,4-benzoquinone 
• 118-92-3 anthranilic acid 
• 121-04-0 toluene-2,4-disulfonic acid 
• 7134-03-4 3-hydroxy-4-methylbenzenesulfonic acid 
• 72856-73-6 2-methoxy-4-(methylsulfanyl)benzoic acid 
• 89469-32-9 4-Chlorosulphonyl-2-methoxybenzoic acid 
• 1613111-26-4 C₇H₇N₂O₃S⁽¹⁺⁾*Cl^(1-) 

Relevant academic research and scientific papers

Synthesis of 2-Methoxy-4-(methylsulfanyl)benzoic Acid — An Intermediate Product in the Preparation of the Cardiotonic Drugs Sulmazole and Isomazole

Readily available 4-methyl-3-nitrobenzenesulfonic acid and 2-methyl-5-nitrophenol were used to develop two alternative approaches to the synthesis of 2-methoxy-4-(methylsulfanyl)benzoic acid in total yields of 17% and 37%, respectively. The synthesis starting from 2-methyl-5-nitrophenol is more process-oriented and can be used in the resynthesis of Sulmazole and Isomazole.

2,4-diamino-6-fluorotriazine disazo reactive dyestuffs

A dyestuff of the formula STR1 in which R is H or Ch3 STR2 in which R1 is H, substituted or unsubstituted C1 -C4 -alkyl or --X--Y X is a divalent aliphatic, cycloaliphatic, aliphaticcycloaliphatic radical or an araliphatic radical Y is COOH, SO3 H, OSO3 H or SO2 G, in which G is CH=CH2 or --CH2 --CH2 --Z, in which Z denotes a group which can be eliminated under alkaline conditions, R2 is H or C1 -C4 -alkyl, and the benzene radical D and the benzene or naphthalene radical L can contain customary substituents, is suitable for the dyeing and printing of OH- and NH-containing materials. They produce lightfast and wetfast brilliant dyeings and prints.

Alkanol substituted disazo orange dye for nylon

The specification describes a new group of alkanol substituted disazo compounds that are useful in dyeing polyamide textile fibers in orange hues. The new compounds are compatible with several acid blue dyes and several acid red dyes that are commercially important as dyes for nylon. The new compounds are particularly well suited for use as the "yellow" component in trichromatic systems for dying polyamide carpeting and other textiles. The new compounds are relatively inexpensive to make and have outstanding application and fastness properties. Other aspects of the specification are concerned with a method of making the new compounds and with a method of dyeing polyamides with said compounds and to the novel dyed polyamides resulting from the use of the new group of compounds as dyes.

Triazinyl reactive dyes containing additional fiber reactive groups bound through the sulfonylalkylaminoalkylamino bridge

The invention relates to novel useful reactive dyes of the formula I STR1 in which: F is a radical selected from the group consisting of metal-free or metal-containing monoazo or disazo dyes containing at least one --SO3 H group, anthraquinone dyes, sulfophthalocyanine dyes, formazan dyes, phenazine dyes, oxanine dyes and nitroaryl dyes, R is hydrogen, C1 -C4 alkyl which is unsubstituted or substituted with --COOH or --SO3 H, cyanoethyl, or hydroxyethyl, X is fluorine, chlorine, bromine, --SO3 H, phenylsulfonyl or C1 -C4 -alkylsulfonyl, P is 1 or 2 and A is a radical of the formula STR2 in which: the groups designated "alk" are independently of each other straight or branched polymethylene radicals having 2 to 6 carbon atoms, and Z is β-halogenoethyl, vinyl, β-sulfatoethyl, β-thiosulfatoethyl or βacetoxyethyl.

Reactive dyestuffs comprising a triazine moiety and a vinylsulfonyl moiety both being linked by a substituted alkylene bridge member

A reactive dye of the formula STR1 in which: F is a radical selected from the group consisting of metal-free or metal-containing monoazo or disazo dyes containing at least one --SO3 H group, anthraquinone dyes, sulfophthalocyanine dyes, formazan dyes, phenazine dyes, oxazine dyes and nitroaryl dyes, R is hydrogen, C1 -C4 alkyl which is unsubstituted or substituted with --COOH or --SO3 H, cyanoethyl, or hydroxyethyl, X is fluorine, chlorine, bromine, --SO3 H, phenylsulfonyl or C1 -C4 -alkylsulfonyl, p is 1 or 2 and A is a radical of the formula STR2 in which: Y is chlorine, bromine, fluorine, --OH, --OSO3 H, --O-acyl, --CN, --COOH, --COO--C1 -C4 -alkyl, --CONH2 or --SO2 --Z, the group designated "alk" is a straight or branched polymethylene radical having 2 to 6 carbon atoms, V is STR3 hydrogen or C1 -C4 -alkyl which is unsubstituted or substituted by C1 -C2 -alkoxy, carboxyl, sulfo, halogen or hydroxy, Z is β-halogenoethyl, vinyl or β-acetoxyethyl, or A is a radical of the formulae STR4 in all of which R' is C1-6 -alkyl or hydrogen, Z is as defined above, o is 0 to 6, and m is 2 to 6.

Barium laked phenylazonaphthalene dye containing sulfonic acid groups

Azo dyes containing sulfonic acid groups laked with barium and derived from an anilinesulfonic acid as diazo component and a β-naphtholsulfonic acid as coupling component for example a dye of the formula STR1 The dyes are eminently suitable as pigments for coloring surface coating compositions, printing inks and particlarly resins.