35975-12-3

Usage

Uses

Used in Hair Dye Industry:
3,6-Dimethyl-1,2-benzendiamine is used as a key ingredient in hair dyes for its capacity to create vibrant and long-lasting colors. It contributes to the effectiveness and quality of hair coloring products, enhancing their performance and consumer satisfaction.
Used in Textile Industry:
In the textile industry, 3,6-Dimethyl-1,2-benzendiamine is utilized as a dye component to impart color to fabrics. Its properties allow for the creation of a wide range of hues, adding aesthetic value and visual appeal to textile products.

InChI:InChI=1/C8H12N2/c1-5-3-4-6(2)8(10)7(5)9/h3-4H,9-10H2,1-2H3

Upstream product

• 711-41-1 2,3-dinitro-p-xylene 
• 106-42-3 para-xylene 
• 623-26-7 terephthalonitrile 
• 95-78-3 2,5-Dimethylaniline 
• 89-58-7 mononitro-p-xylene 
• 15540-85-9 2,5-dimethyl-6-nitroaniline 

Downstream Products

• 101102-39-0 4,7-dimethylbenzimidazole 
• 108468-00-4 tert-butyl 4-(aminomethyl)benzylcarbamate 
• 69272-53-3 2-Chlor-4,7-dimethyl-benzimidazol 
• 1375277-78-3 (S)-N-(benzo[d][1,3]dioxol-5-yl)-2-(2-(3-ethyl-4,7-dimethyl-2-oxo-2,3-dihydrobenzo[d]imidazol-1-yl)acetamido)-N-methyl-3-phenylpropanamide 
• 69272-51-1 4,7-dimethyl-1,3-dihydro-benzoimidazol-2-one 
• 25798-65-6 4,7-dimethyl-2-phenyl-1H-benzo[d]imidazole 
• 67468-93-3 2-Amino-4,7-dimethylbenzimidazol 
• 89265-25-8 2,3-diiodo-1,4-bis(bromomethyl)benzene 

Relevant academic research and scientific papers

Mechanism-Inspired Design of Bifunctional Catalysts for the Alternating Ring-Opening Copolymerization of Epoxides and Cyclic Anhydrides

Advances in catalysis have enabled the ring-opening copolymerization of epoxides and cyclic anhydrides to afford structurally and functionally diverse polyesters with controlled molecular weights and dispersities. However, the most common systems employ b

Synthesis of ortho-phenylenebis(guanidine) derivatives with potential chirality

We report the synthesis and potential chirality of ortho-phenylenebisguanidines (BGs) with substituents at C(3) and C(6). Guanidinylation of 3,6-disubstituted benzene-1,2-diamines with 2-chloro-4,5-dihydro-1,3-dimethyl-1H-imidazolium chloride gave the corresponding BGs. X-Ray crystallography showed that the two guanidine moieties occupy different faces of the benzene ring, creating potential chirality, although optical resolution of tBu-substituted BG by chiral HPLC failed. However, a methylated acyclic bisguanidinium salt (BGms) was obtained as a chiral crystal with a space group of P212121.

Asymmetric Hydrogenation of 3,5-Bistrifluoromethyl Acetophenone in Pilot Scale with Industrially Viable Ru/Diphosphine-Benzimidazole Complexes

A novel efficient asymmetric hydrogenation (AH) process was developed for the preparation of (R)-1-(3,5-bis(trifluoromethyl)phenyl)ethanol (3), using a catalyst Ru/(4R,5R)-(+)-4,5-bis(diphenylphosphinomethyl)-2,2-dimethyl-1,3-dioxoane-(R,R-Diop)-2R-(α-met

NOVEL ANTIVIRAL COMPOUNDS

The present invention relates to a compound of formula I: or a pharmaceutically acceptable salt thereof, wherein the symbols are as defined in the specification; a pharmaceutical composition comprising the same, a method for treating or preventing a viral infection such as HIV using the same.

Catalysts and process for producing aromatic amines

As catalysts for producing aromatic amines by hydrogenating aromatic nitrites, there are disclosed (1) the catalyst comprising a metal catalyst component comprising Ni and/or Co and a specific amount of zirconia as a carrier component, which is prepared b

Process for preparing cyano group-containing aromatic methylamines

PCT No. PCT/JP98/00464 Sec. 371 Date Sep. 30, 1998 Sec. 102(e) Date Sep. 30, 1998 PCT Filed Feb. 4, 1998 PCT Pub. No. WO98/33767 PCT Pub. Date Aug. 6, 1998The object of the invention is to provide a process for preparing a cyano group-containing methylamine, comprising hydrogenating only one of the two nitrile groups of a aromatic dinitrile, wherein the aromatic dinitrile is reacted a a high conversion ratio using a small amount of a catalyst under the conditions of a low temperature and a low pressure to prepare a cyano group-containing aromatic methylamine in a high yield.

Photocyclisations of Unsaturated 4>Paracyclophanes

The photocyclisation of 4>paracyclophanes with one or two unsaturated bridges, compounds 7 and 3, gives 3>(3,6)phenanthrenodiparacyclophane, 8, and 2>(2,13)pentahelicenoparacyclophane, 4, respectively.In contrast, 2

Ethylenic silicon compounds and thermoplastic elastomers obtained therefrom

The invention provides organosilicon compounds of the formula: STR1 in which: N IS 1, 2 OR 3; Each R, which may be identical or different, is a monovalent organic group which contains a carbon-carbon double bond and from 2 to 10 carbon atoms; Each R1, which may be identical or different, is a straight or branched alkyl radical optionally substituted by one or more halogen atoms or cyano groups; an aryl radical or an alkylaryl radical optionally substituted by one or more halogen atoms; R2 is a straight or branched divalent alkylene or alkylidene radical possessing up to 4 carbon atoms; X is a divalent radical consisting of, or containing, at least one hetero-atom selected from oxygen, sulphur and nitrogen atoms, the radical being attached to the radical R2 via a said hetero-atom; G is an organic radical of valency (m+ l) possess from 1 to 30 carbon atoms; m is 1, 2 or 3; And each Y, which may be identical or different, is a functional group selected from: --NO2, STR2 --COOM (where M represents a sodium, potassium or lithium atom); --COOR4 ; STR3 --COCl; --OH; --OR4 ; STR4 --SH; --SR4 ; STR5 --CONH2 ; --CSNH2 ; --CN; --CH2 --NH2 ; --CHO; STR6 --NCO; STR7 wherein R3 represents a hydrogen atom or a straight or branched alkyl radical possessing up to 6 carbon atoms and R4 represents an alkyl radical possessing up to 4 carbon atoms, with the proviso that two Y groups can together constitute an imide group STR8 wherein R5 represents a hydrogen atom or a straight or branched alkyl radical possessing up to 4 carbon atoms. These are useful intermediates in the preparation of disilanes and silicon polymers, in particular of polyethylenic silicon compounds which can be polymerized with an α, ω-dihydrogenopolysiloxane to give thermoplastic elastomers.