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4-amino-3,5-dimethyl-benzenesulfonic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20804-27-7

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20804-27-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20804-27-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,8,0 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 20804-27:
(7*2)+(6*0)+(5*8)+(4*0)+(3*4)+(2*2)+(1*7)=77
77 % 10 = 7
So 20804-27-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H11NO3S/c1-5-3-7(13(10,11)12)4-6(2)8(5)9/h3-4H,9H2,1-2H3,(H,10,11,12)

20804-27-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-amino-3,5-dimethylbenzenesulfonic acid

1.2 Other means of identification

Product number -
Other names 2.6-Dimethylanilin-4-sulfonsaeure

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:20804-27-7 SDS

20804-27-7Relevant academic research and scientific papers

Palladium-catalyzed aerobic alcohol oxidation supported by a new type of α-diimine ligands

Zhou, Jin,Li, Xiaoyan,Sun, Hongjian

, p. 782 - 790 (2008)

A series of new ionic sulfonated α-diimine ligands were prepared and employed as supporting ligands for the palladium-catalyzed aerobic alcohol oxidation. The electronic properties, rigidity, and steric hindrance of ligands have remarkable influences upon the catalytic activity of the palladium complexes. The best catalytic result could be achieved using ligand 9 with an electron-withdrawing sulfonyl substituent together with bulky groups (iso-propyl in 2,6-positions). This diimine/palladium-catalyzed system is highly efficient for the oxidation of various benzylic alcohols, and showed moderate yields for the secondary aliphatic alcohols and cyclic alcohols.

Sulfonated N-heterocyclic carbenes for Suzuki coupling in water

Fleckenstein, Christoph,Roy, Sutapa,Leuthaeusser, Steffen,Plenio, Herbert

, p. 2870 - 2872 (2007)

Sulfonated, water-soluble imidazolium and imidazolinium salts were synthesized and the respective Pd-complexes with N,N′-bis(2,6-dialkyl-4- SO3--phenyl)imidazol-2-ylidene and N,N′-bis(2,6- dialkyl-4-SO3--phenyl)-4,5-dihydroimidazol-2-ylidene ligands were applied in aqueous Suzuki coupling reactions of aryl chlorides. The Royal Society of Chemistry.

Nitroso compounds and their use as spin traps

-

, (2008/06/13)

A compound of the formula wherein X is Cl or CH3, or a salt thereof, is useful as a spin trap in various assays.

Nitroso compounds and their use as spin traps

-

Page column 4, (2008/06/13)

A compound of the formula wherein X is Cl or CH3, or a salt thereof, is useful as a spin trap in various assays.

On the intermediacy of phenyl hydrogen sulfates in the sulfonation of phenols. Sulfonation of phenol, anisole, methyl phenyl sulfate, the 2-halogenophenols, a series of phenyl methanesulfonates together with 2,6-dimethylaniline and its N-methylsulfonyl derivative

de Wit, Peter,Woldhuis, Alex F.,Cerfontain, Hans

, p. 668 - 675 (2007/10/02)

The sulfonation of methyl phenyl sulfate (4) with concentrated aqueous sulfuric acid at 25 deg C yields the 4-sulfonic acid.This initial product then decomposes to give phenol-4-sulfonic acid, which is subsequently sulfonated to phenol-2,4-disulfonic acid.From the first-order-rate coefficients obtained for sulfonation of phenyl methanesulfonate (3) and (4) in 93,2percent H2SO4, for which acid concentration the sulfonating entity is H2S2O7, the ?p+ values of the OSO2Me and OSO2OMe substituents have been determined to be 0.40 and 0.46, respectively.The sulfonation of both 2-chlorophenyl (10) and 2-methylphenyl methanesulfonate (14) with 2.0 equiv of SO3 in nitromethane at 0.0 deg C yields the 4-sulfonic acid as the exclusive product, whereas 2-methoxyphenyl methanesulfonate (13), under the same conditions, forms exclusively the 5-sulfonic acid. 2-Chloro- (6), 2-bromo- (7) and 2-iodophenol (8) with 1.0 and 4.0 equiv of SO3 in nitromethane yield exclusively the 4-sulfonic acid, while 2-fluorophenol (5) with 2.0 and 5.0 equiv of SO3 yields in addition the 5-sulfonic acid to the extent of 4 and 30percent, respectively.In the reactions of 2,6-dimethylphenol (15) and 2,6-dimethylaniline (17) with at least 1 equiv of SO3 in nitromethane, the 3-SO3H/4-SO3H ratio was found to increase on increasing the relative amount of SO3.For both 15 and 17, the limiting 3-SO3H/4-SO3H ratio at high SO3/ArOH ratios is 86/14 and this value is considered to be the ratio for the sulfonation of both 2,6-dimethylphenyl hydrogen sulfate and 2,6-dimethylaniline-N-sulfonic acid.This assumption is supported by the observation that the sulfonation of 2,6-dimethylphenyl methanesulfonate (16) and N-(methylsulfonyl)-2,6-dimethylaniline (18) with SO3 leads to a similar 3-SO3H/4-SO3H ratio.

Studies of Reactions of Amines with Sulfur Trioxide. VI. Thermal Reactions of Anilinium, Dimethylanilinium, and Trimethylanilinium Salts of Butylamidosulfuric Acid

Kanetani, Fujio,Yamaguchi, Hachiro

, p. 3048 - 3058 (2007/10/02)

When the title compounds were heated in an evacuated reaction vessel, both transsulfonation and rearrangement occurred.At lower temperatures (80-120 deg C) the corresponding phenylamidosulfates and sulfophenylamidosulfates (transsulfonation products) were the main products.Increasing temperature led to the formation of ring mono- and disulfonates (rearrangement products) at the expense of the transsulfonation products.The sulfonate group always migrated to the ortho and/or para position(s) to the amino group.In no case was any meta-product detected.There was no significant difference in the ease of transsulfonation among the anilinium salts studied exept 2,6-dimethyl- and 2,4,6-trimethylanilinium salts.On the other hand, the ease of rearrangement and the orientation of ring sulfonation depended strongly on the structure of the substrate anilines.The thermal reactions of 2,4,6-trimethylanilinium butylamidosulfate produced (2,4,6-trimethylphenylimido)bis(sulfate) in addition to (2,4,6-trimethylphenylamido)sulfate.This is the first isolation of an arylimidobis(sulfate) from such reactions.Mechanisms of the transsulfonation and rearrangement have been discussed.

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