632-46-2

Basic information

• Product Name: 2,6-Dimethylbenzoic acid
• Synonyms: M-XYLENE-2-CARBOXYLIC ACID;TIMTEC-BB SBB007881;RARECHEM AL BO 0401;VIC-M-XYLYLIC ACID;2,6-dimethyl-benzoicaci;2,6-DIMETHYLBENZOIC ACID;Benzoic acid, 2,6-dimethyl- (7CI,8CI,9CI);Benzoic acid, 2,6-dimethyl-
• CAS NO: 632-46-2
• Molecular Formula: C₉H₁₀O₂
• Molecular Weight: 150.17
• EINECS: 211-177-0
• Product Categories: CARBOXYLICACID;Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;Benzoic acid;Benzoic acid Series;Aromatics;Intermediates & Fine Chemicals;Pharmaceuticals
• Mol File: 632-46-2.mol
• Article Data: 25

Chemical Properties

• Melting Point: 114-116 °C(lit.)
• Boiling Point: 160 °C / 17mmHg
• Flash Point: 126.126 °C
• Appearance: White to pale cream/Crystalline Powder
• Density: 1.0937 (estimate)
• Vapor Pressure: 0.003mmHg at 25°C
• Refractive Index: 1.5236 (estimate)
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: pKa: 3.362(25°C)
• BRN: 1863791
• CAS DataBase Reference: 2,6-Dimethylbenzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-Dimethylbenzoic acid(632-46-2)
• EPA Substance Registry System: 2,6-Dimethylbenzoic acid(632-46-2)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36-24/25
• WGK Germany: 3
• RTECS: DG8734010
• Hazardous Substances Data: 632-46-2(Hazardous Substances Data)

Usage

Uses

Different sources of media describe the Uses of 632-46-2 differently. You can refer to the following data:
1. 2,6-Dimethylbenzoic acid is a benzoic acid derivative used in the preparation of antiinflammatory and antirheumatic agents. And it is also a potential geothermal tracer.
2. Benzoic acid derivative used in the preparation of antiinflammatory and antirheumatic agents. A potential geothermal tracer.

Definition

ChEBI: A dimethylbenzoic acid in which the two methyl groups are located at positions 2 and 6.

General Description

Crystal structure of 2,6-dimethylbenzoic acid was studied by three-dimensional X-ray methods.

Purification Methods

Steam distil the acid, and crystallise it from EtOH or H2O (m 116.3-116.7o). The N-dimethylamide has m 62-63o (from Et2O). [Beilstein 9 H 531, 9 IV 1798.]

InChI:InChI=1/C9H10O2/c1-6-4-3-5-7(2)8(6)9(10)11/h3-5H,1-2H3,(H,10,11)

Synthetic route

4-methoxybenzyl 2,6-dimethylbenzoate + ethylene glycol (107-21-1) → 2,6-dimethylbenzoic acid (632-46-2) + 2-(4-methoxybenzyloxy)ethanol (13807-89-1)

Conditions	Yield
at 140℃; for 4h;	A 96% B n/a

carbon dioxide (124-38-9) + 2-Bromo-m-xylene (576-22-7) → 2,6-dimethylbenzoic acid (632-46-2)

Conditions	Yield
Stage #1: 2-Bromo-m-xylene With n-butyllithium In tetrahydrofuran; hexane at -78℃; for 1h; Inert atmosphere; Stage #2: carbon dioxide In tetrahydrofuran; hexane at -78 - 20℃;	93.2%
Stage #1: 2-Bromo-m-xylene With ethyl bromide; magnesium In diethyl ether Grignard reaction; Inert atmosphere; Reflux; Stage #2: carbon dioxide In diethyl ether at 20℃; Grignard reaction; Inert atmosphere;	54%
(i) Mg, (ii) /BRN= 1900390/; Multistep reaction;
(i) Mg, EtBr, Et2O, (ii) /BRN= 1900390/; Multistep reaction;

carbon dioxide (124-38-9) + 2,6-dimethylbenzene boronic acid (100379-00-8) → 2,6-dimethylbenzoic acid (632-46-2)

Conditions	Yield
With chloro[1,3-bis(2,6-di-i-propylphenyl)imidazol-2-ylidene]copper(I); potassium methanolate In tetrahydrofuran at 70℃; for 24h; Schlenk technique; Sealed tube;	88%

dicobalt octacarbonyl (15226-74-1, 61091-28-9, 61117-58-6) + 2,6-dimethylphenyl trifluoromethanesulphonate (86364-02-5) → 2,6-dimethylbenzoic acid (632-46-2)

Conditions	Yield
With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; potassium acetate In 1,4-dioxane; water at 50℃; for 12h; Schlenk technique; Inert atmosphere; chemoselective reaction;	82%

2,6-dimethyl-N-(quinolin-8-yl)benzamide (1609401-42-4) → 2,6-dimethylbenzoic acid (632-46-2)

Conditions	Yield
With sulfuric acid; water at 120℃; for 24h;	80%

dicobalt octacarbonyl (15226-74-1, 61091-28-9, 61117-58-6) + 2,6-dimethylphenyl 2,3,4,5,6-pentafluorobenzenesulfonate → 2,6-dimethylbenzoic acid (632-46-2)

Conditions	Yield
With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; potassium acetate In 1,4-dioxane; water at 50℃; for 12h; Schlenk technique; Inert atmosphere; chemoselective reaction;	79%

ortho-methylbenzoic acid (118-90-1) + dihydroxy-methyl-borane (13061-96-6) → 2,6-dimethylbenzoic acid (632-46-2)

Conditions	Yield
With dipotassium hydrogenphosphate; silver carbonate; p-benzoquinone; palladium diacetate In tert-butyl alcohol at 100℃; for 3h;	75%

carbon dioxide (124-38-9) + C10H14Si → 2,6-dimethylbenzoic acid (632-46-2)

Conditions	Yield
Stage #1: carbon dioxide With bis(1,5-cyclooctadiene)nickel (0); 1,3-bis-(2,6-diisopropylphenyl)-imidazol-2-ylidene In 1,3,5-trimethyl-benzene at 20℃; under 760.051 Torr; for 0.166667h; Schlenk technique; Stage #2: C10H14Si In 1,3,5-trimethyl-benzene at 160℃; for 20h; Schlenk technique;	58%

dihydroxy-methyl-borane (13061-96-6) + sodium o-toluate (17264-71-0) → 2,6-dimethylbenzoic acid (632-46-2)

Conditions	Yield
With silver carbonate; p-benzoquinone; palladium diacetate In tert-butyl alcohol at 100℃; for 3h;	50%

dihydroxy-methyl-borane (13061-96-6) + 2-methylbenzoic acid potassium salt (16463-31-3) → 2,6-dimethylbenzoic acid (632-46-2)

Conditions	Yield
With silver carbonate; p-benzoquinone; palladium diacetate In tert-butyl alcohol at 100℃; for 3h;	48%

ortho-methylbenzoic acid (118-90-1) + di-tert-butyl peroxide (110-05-4) → 2,6-dimethylbenzoic acid (632-46-2)

Conditions	Yield
With potassium acetate; palladium diacetate at 80℃; under 760.051 Torr; for 24h;	48%
With potassium acetate; palladium diacetate at 80℃; for 24h; Schlenk technique;	48%

2-fluoro-m-xylene (443-88-9) + carbon dioxide (124-38-9) → 2,6-dimethylbenzoic acid (632-46-2)

Conditions	Yield
Stage #1: 2-fluoro-m-xylene With C78H70Al2Cl4N6P4Rh2; magnesium; ethylene dibromide In tetrahydrofuran at 50℃; for 22h; Inert atmosphere; Glovebox; Stage #2: carbon dioxide In tetrahydrofuran at 20℃; under 760.051 Torr; for 0.5h;	48%

1,2,3-trimethylbenzene (526-73-8) → 2,6-dimethylbenzoic acid (632-46-2) + 2,3-dimethylbenzoic acid (603-79-2)

Conditions	Yield
With air; acetic acid; 1N,3N,5N-trihydroxy-1,3,5-triazin-2,4,6[1H,3H,5H]-trione; cobalt(II) acetate; manganese(II) acetate at 100℃; under 760 Torr; for 1h;	A 13% B 36%

carbon monoxide (201230-82-2) + 2,6-dimethylbenzenediazonium tetrafluoroborate (2192-33-8) → 2,6-dimethylbenzoic acid (632-46-2) + N-(2,6-dimethylphenyl)acetamide (2198-53-0) + 2,6-Dimethylbenzoic anhydride (73368-14-6)

Conditions	Yield
With sodium acetate; palladium diacetate In acetonitrile under 6619.6 Torr; for 1h; Ambient temperature;	A 28% B 16% C 3%

2,5-dimethylbenzamide (55321-98-7) → 2,6-dimethylbenzoic acid (632-46-2)

Conditions	Yield
With phosphoric acid at 145 - 150℃;

4-amino-2,6-dimethyl benzoic acid (16752-16-2) → 2,6-dimethylbenzoic acid (632-46-2)

Conditions	Yield
Diazotization.Reaktion ueber mehrere Stufen;

2,2,2-trichloro-1-(2,6-dimethyl-phenyl)-ethanone (99184-32-4) → 2,6-dimethylbenzoic acid (632-46-2) + (2,6-dimethyl-phenyl)-hydroxy-acetic acid (99186-43-3)

Conditions	Yield
With sodium hydroxide

(2,6-dimethyl-benzyl)-dimethyl-amine (54521-25-4) → 2,6-dimethylbenzoic acid (632-46-2)

Conditions	Yield
With sodium hydroxide; potassium permanganate

2,6-dimethylbenzoyl chloride (21900-37-8) → 2,6-dimethylbenzoic acid (632-46-2)

Conditions	Yield
With water In acetone at -20℃; Rate constant;

2,6-dimethylaniline (87-62-7) → 2,6-dimethylbenzoic acid (632-46-2)

Conditions	Yield
1) diazotation; Multistep reaction;
Multi-step reaction with 2 steps 1: (i) (diazotization), aq. HBr, (ii) Cu 2: (i) Mg, (ii) /BRN= 1900390/ View Scheme
Multi-step reaction with 2 steps 1: (i) NaNO2, aq. HBr, (ii) CuBr 2: (i) Mg, EtBr, Et2O, (ii) /BRN= 1900390/ View Scheme
Multi-step reaction with 2 steps 1: (i) NaNO2, aq. HCl, (ii) /BRN= 4652394/, CuSO4, aq. NH3, benzene 2: aq. H2SO4 / Heating View Scheme

bis(2,6-dimethylbenzoyl) peroxide (96436-29-2) → 2,6-dimethylbenzoic acid (632-46-2) + m-xylene (108-38-3) + 2,6-dimethylphenyl 2,6-dimethylbenzoate

Conditions	Yield
With 2,4,6-tri-tert-butylphenoxol In acetonitrile Ambient temperature; Irradiation; laser flash photolyses with 308-nm laser puses; Yield given. Yields of byproduct given;
With 2,4,6-tri-tert-butylphenoxol In acetonitrile Ambient temperature; Irradiation; Yield given. Yields of byproduct given;
In acetonitrile Product distribution; Mechanism; Irradiation; in the presence or absence of 2,4,6-tri-tert-butylphenol and/or dibenzoyl peroxide; structural and solvent effect upon decarboxylation investigated of various 2,6-disubstituited benzoyloxy radicals;

ethanol (64-17-5) + 2,6-dimethylbenzoyl chloride (21900-37-8) → 2,6-dimethylbenzoic acid (632-46-2) + 2,6-dimethylbenzoic acid ethyl ester (36596-67-5)

Conditions	Yield
With water at 10℃; Kinetics; Thermodynamic data; Product distribution; solvolysis examined; var. solvents and ratio of ones; mechanism; ΔH(excit.), ΔS(excit.);

2,6-dimethyliodobenzene (608-28-6) + carbon dioxide (124-38-9) → 2,6-dimethylbenzoic acid (632-46-2)

Conditions	Yield
(i) Mg, EtBr, I2, (ii) /BRN= 1900390/; Multistep reaction;

2,6-dimethylbenzonitrile (6575-13-9) → 2,6-dimethylbenzoic acid (632-46-2)

Conditions	Yield
With sulfuric acid Heating;
Multi-step reaction with 2 steps 1: concentrated sulfuric acid / 75 - 80 °C 2: phosphoric acid / 145 - 150 °C View Scheme

4-chloro-2,6-dimethyl benzoic acid (35887-72-0) → 2,6-dimethylbenzoic acid (632-46-2)

Conditions	Yield
With sodium hydroxide; nickel

methanol (67-56-1) + methyl 2,6-dimethylbenzoate (14920-81-1) → 7-methyl-3H-isobenzofuran-1-one (2211-84-9) + 2,6-dimethylbenzoic acid (632-46-2) + 2-Methoxymethyl-6-methylbenzoesaeure

Conditions	Yield
With sodium hydroxide; N-Bromosuccinimide 1.) CCl4, reflux, 3 h, irradiation, 2.) reflux, 35 h; Yield given. Multistep reaction. Yields of byproduct given;

methylammonium carbonate (15719-64-9, 15719-76-3, 97762-63-5) + 2,6-dimethyl-phenyl magnesium bromide → 2,6-dimethylbenzoic acid (632-46-2)

methylammonium carbonate (15719-64-9, 15719-76-3, 97762-63-5) + 2,6-dimethyl-phenyl magnesium iodide → 2,6-dimethylbenzoic acid (632-46-2)

diazotized 2-amino-m-xylene + potassium cuprocyanide → 2,6-dimethylbenzoic acid (632-46-2)

Conditions	Yield
durch Verseifung;

2,6-dimethylbenzoic acid (632-46-2) → 2,6-dimethylbenzyl alcohol (62285-58-9)

Conditions	Yield
With Trimethyl borate; dimethylsulfide borane complex In tetrahydrofuran for 72h; Ambient temperature;	100%
Stage #1: 2,6-dimethylbenzoic acid With borane-THF In tetrahydrofuran at 0 - 20℃; for 64.3333h; Stage #2: With methanol In tetrahydrofuran	99%
With borane-THF In tetrahydrofuran at 0 - 20℃; for 64.3h;	99%

2,6-dimethylbenzoic acid (632-46-2) + dimethyl sulfate (77-78-1) → methyl 2,6-dimethylbenzoate (14920-81-1)

Conditions	Yield
With potassium carbonate In acetone at 20℃;	100%
With potassium carbonate In acetone at 20℃; for 4h;	93%
With potassium hydroxide
With potassium carbonate at 25℃; for 1h;

2,6-dimethylbenzoic acid (632-46-2) + methylamine (74-89-5) → 2,6-dimethyl-N-methylbenzamide (223554-22-1)

Conditions	Yield
	100%

2,6-dimethylbenzoic acid (632-46-2) + C82H102N4O28Pt8 → C124H138N4O28Pt8

Conditions	Yield
In methanol; dichloromethane at 20℃; for 6h;	100%

2,6-dimethylbenzoic acid (632-46-2) + tetramethyl ammoniumhydroxide (75-59-2) → C9H9O2(1-)*C4H12N(1+)

Conditions	Yield
With water In ethanol at 0 - 20℃; for 0.0833333h;	100%

2,6-dimethylbenzoic acid (632-46-2) + 1-ethoxyacetylene (927-80-0) → 2,6-Dimethyl-benzoic acid 1-ethoxy-vinyl ester

Conditions	Yield
With [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2 In toluene at 0 - 20℃; for 5h;	99.9%

norborn-2-ene (498-66-8) + 2,6-dimethylbenzoic acid (632-46-2) → C8H11O2C6H5CH2CH2

Conditions	Yield
silver trifluoromethanesulfonate; iron(III) chloride In 1,2-dichloro-ethane at 80℃;	99%

2,6-dimethylbenzoic acid (632-46-2) + diphenyl acetylene (501-65-5) → C23H20O2

Conditions	Yield
With [{Au(IPr)}2(μ-OH)][BF4] In neat (no solvent) at 80℃; for 15h; regioselective reaction;	99%

2,6-dimethylbenzoic acid (632-46-2) → 2,6-dimethyl-3-nitrobenzoic acid (6307-70-6)

Conditions	Yield
With sulfuric acid; nitric acid at 0℃; for 1.5h;	98%
With sulfuric acid; nitric acid at 0℃; for 1h;
With nitric acid; acetic acid In (2S)-N-methyl-1-phenylpropan-2-amine hydrate; sulfuric acid

2,6-dimethylbenzoic acid (632-46-2) + cyanoacetic acid (372-09-8) → cyanomethyl 2,6-dimethylbenzoate

Conditions	Yield
With tert.-butylhydroperoxide; sodium acetate; tetra-(n-butyl)ammonium iodide In tetrahydrofuran; water at 80℃; for 12h;	98%
With tert.-butylhydroperoxide; sodium acetate; tetra-(n-butyl)ammonium iodide In tetrahydrofuran; water at 80℃; for 12h;	96%

2,6-dimethylbenzoic acid (632-46-2) + methyl iodide (74-88-4) → methyl 2,6-dimethylbenzoate (14920-81-1)

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 24h; Inert atmosphere;	97%
With potassium carbonate In N,N-dimethyl-formamide at 0 - 25℃; for 5h; Inert atmosphere;	95%
With potassium carbonate In N,N-dimethyl-formamide at 0 - 20℃; for 16h; Inert atmosphere;	89%

styrene (292638-84-7) + 2,6-dimethylbenzoic acid (632-46-2) → 2-bromo-1-phenylethyl 2,6-dimethylbenzoate

Conditions	Yield
With C19H27NO2 In n-heptane at 23℃; Darkness; Green chemistry;	97%
With N-Bromosuccinimide; C25H44NO2PS In chloroform at 25℃; for 20h; Darkness; regioselective reaction;	90%

2,6-dimethylbenzoic acid (632-46-2) + N-Cyclohexyl-2-hydroxy-2-(S)-pyrrolidin-2-yl-acetamide; hydrochloride → N-cyclohexyl-(RS)-2-hydroxy-2-{(S)-2-[1-(2,6-dimethylbenzoyl)pyrrolidinyl]}acetamide

Conditions	Yield
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In N,N-dimethyl-formamide Ambient temperature;	96.3%

2,6-dimethylbenzoic acid (632-46-2) → 2,6-dimethylcyclohexa-2,5-diene-1-carboxylic acid (31673-42-4)

Conditions	Yield
With ammonia; sodium In ethanol at -50℃; Birch reduction;	96%
With tert-Amyl alcohol; lithium In tetrahydrofuran; ammonia Birch Reduction; Reflux; liquid NH3;	90%
With N,N'-Dimethylurea; tris(pyrrolidino)phosphine oxide; lithium bromide In tetrahydrofuran Electrochemical reaction;	90%

2,6-dimethylbenzoic acid (632-46-2) → 2,6-Dimethylbenzoic anhydride (73368-14-6)

Conditions	Yield
With 2,6-dimethylpyridine; tris(2,2'-bipyridyl)ruthenium dichloride; carbon tetrabromide; N,N-dimethyl-formamide at 25 - 30℃; for 12h; Inert atmosphere; Photolysis;	96%
With potassium carbonate; p-toluenesulfonyl chloride In dichloromethane; acetonitrile at 20℃; for 48h;	94%
With copper(II) bis(trifluoromethanesulfonate) at 80℃; for 0.5h;	81%

ethanol (64-17-5) + 2,6-dimethylbenzoic acid (632-46-2) → 2,6-dimethylbenzoic acid ethyl ester (36596-67-5)

Conditions	Yield
With sulfuric acid at 100℃; for 12h; Sealed tube;	95%

2,6-dimethylbenzoic acid (632-46-2) + (R)-[1-(naphthalen-2-yl)ethyl]amine (1201-74-7, 3082-62-0, 3906-16-9, 64234-21-5) → 2,6-dimethyl-N-[(R)-1-(2-naphthyl)ethyl]benzamide (1184301-95-8)

Conditions	Yield
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 0 - 23℃; Combinatorial reaction / High throughput screening (HTS); Inert atmosphere;	94%

2,6-dimethylbenzoic acid (632-46-2) + propionyl chloride (79-03-8) → 2,6-dimethylbenzoic propionic anhydride

Conditions	Yield
With triethylamine In tetrahydrofuran at 0 - 20℃; Inert atmosphere;	94%

2,6-dimethylbenzoic acid (632-46-2) + 2,3-dimethyl-N-(quinolin-8-yl)benzamide → 3,4-dimethyl-2-(quinolin-8-ylcarbamoyl)phenyl 2,6-dimethylbenzoate

Conditions	Yield
With silver carbonate; cobalt acetylacetonate In 1,2-dichloro-ethane at 100℃; for 3h;	94%

2,6-dimethylbenzoic acid (632-46-2) + carbonic acid dimethyl ester (616-38-6) → methyl 2,6-dimethylbenzoate (14920-81-1)

Conditions	Yield
With tributyl-amine In N,N-dimethyl-formamide at 285℃; under 112511 Torr; for 0.05h;	93%
With sulfuric acid at 80 - 85℃; for 8h; Neat (no solvent);	74.5%

1-ethenyl-4-methylbenzene (622-97-9) + 2,6-dimethylbenzoic acid (632-46-2) → 2-bromo-1-(p-tolyl)ethyl 2,6-dimethylbenzoate

Conditions	Yield
With C19H27NO2 In n-heptane at 23℃; Darkness; Green chemistry;	93%

2,6-dimethylbenzoic acid (632-46-2) + 3-methoxy-2-methyl-N-(quinolin-8-yl)benzamide → 4-methoxy-3-methyl-2-(quinolin-8-ylcarbamoyl)phenyl 2,6-dimethylbenzoate

Conditions	Yield
With silver carbonate; cobalt acetylacetonate In 1,2-dichloro-ethane at 100℃; for 3h;	92%

4-vinylbenzyl chloride (1073-67-2) + 2,6-dimethylbenzoic acid (632-46-2) → 2-bromo-1-(4-chlorophenyl)ethyl 2,6-dimethylbenzoate

Conditions	Yield
With C19H27NO2 In n-heptane at 23℃; Darkness; Green chemistry;	92%

alpha-D-glucopyranose (492-62-6) + 2,6-dimethylbenzoic acid (632-46-2) → 1-O-(2,6-dimethylbenzoyl)-β-D-glucopyranoside

Conditions	Yield
With di-isopropyl azodicarboxylate; triphenylphosphine In 1,4-dioxane at 20℃; for 0.5h; Mitsunobu Displacement; Inert atmosphere; stereoselective reaction;	92%

2,6-dimethylbenzoic acid (632-46-2) + C21H38BrN3O4 → C30H47N3O6

Conditions	Yield
With potassium fluoride In acetonitrile at 20℃; for 12h; Cooling with ice;	91%

1-bromo-4-ethenyl-benzene (2039-82-9) + 2,6-dimethylbenzoic acid (632-46-2) → 2-bromo-1-(4-bromophenyl)ethyl 2,6-dimethylbenzoate

Conditions	Yield
With C19H27NO2 In n-heptane at 23℃; Darkness; Green chemistry;	91%

Methyl trichloroacetate (598-99-2) + 2,6-dimethylbenzoic acid (632-46-2) → methyl 2,6-dimethylbenzoate (14920-81-1)

Conditions	Yield
With 18-crown-6 ether; potassium carbonate at 90 - 150℃; for 2h;	90%

1,4-dioxane (123-91-1) + 2,6-dimethylbenzoic acid (632-46-2) → C13H16O4 (1284251-40-6)

Conditions	Yield
With tert.-butylhydroperoxide; tetra-(n-butyl)ammonium iodide In water; ethyl acetate at 80℃; for 12h;	90%

Upstream product

• 16752-16-2 4-amino-2,6-dimethyl benzoic acid 
• 21900-37-8 2,6-dimethylbenzoyl chloride 
• 67-56-1 methanol 
• 14920-81-1 methyl 2,6-dimethylbenzoate 
• 92114-96-0 mercury fulminate 
• 108-38-3 m-xylene 
• 861555-63-7 2,6-dimethyl-cyclohexa-1,5-dienecarboxylic acid 
• 7732-18-5 water 
• 526-73-8 1,2,3-trimethylbenzene 
• 7499-18-5 2,6-dimethyl-terephthalamic acid 
• 124-38-9 carbon dioxide 
• 100379-00-8 2,6-dimethylbenzene boronic acid 
• 21450-64-6 (2,6-dimethylphenyl)magnesium bromide 
• 6575-13-9 2,6-dimethylbenzonitrile 

Downstream Products

• 14920-81-1 methyl 2,6-dimethylbenzoate 
• 36596-67-5 2,6-dimethylbenzoic acid ethyl ester 
• 7112-17-6 2c,6c-dimethyl-cyclohexane-r-carboxylic acid 
• 886853-06-1 2,6-dimethyl-3-[(nitrooxy)methyl]benzoic acid 
• 65399-02-2 7-Methyl-2,3-dihydroisoindole-1-one 
• 149228-90-0 2-Azidomethyl-6,N-dimethylbenzamide 
• 149228-91-1 2-Azidomethyl-N-hydroxymethyl-6,N-dimethylbenzamide 
• 149228-89-7 2-Bromomethyl-6-methylbenzoic acid 4-nitrophenyl ester 
• 149228-81-9 2-Azidomethyl-6-methylbenzoic acid 4-nitrophenyl ester 
• 149261-38-1 <(2-Azidomethyl-6-methylbenzoyl)(methyl)amino>methyl-2-(<(tert-butoxy)carbonyl>amino)-3-phenylpropanoate 
• 147566-73-2 tert-butyl 2,6-bis((3,5-diethoxycarbonylphenoxy)methyl)benzoate 

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