As a leading manufacturer and supplier of chemicals in China, DayangChem not only supply popular chemicals, but also DayangChem’s R&D center offer custom synthesis according to the contract research and development services for t
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inquiryWelcome to Simagchem, your partner in China as a premier supply of bulk specialty chemicals for industry and life science. We introduce experienced quality product and exceptional JIT service with instant market intelligence in China to benefit our
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inquiryItems Standard Result Assay (Ursolic acid) 98%min 98.22% ----------------------------------------------------------------
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inquiryProduct description: Product name 2,4,6-Tribromophenol CAS number 118-79-6 Assay ≥99% Appearance White crystalline powder Capacity 500mt/year Application Flame retardant
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inquiry1. Factory price and high quality must be guaranteed, base on 8 years of production and R&D experience 2. Free samples will be provided,ensure specifications and quality are right for customer 3. Customers will receive the most professional techn
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inquiryhigh quality Appearance:White or off-white Solid Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea Port:shanghai
The above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi
Our main production base is located in Xuzhou industry park. We are certified both to the ISO 9001 and ISO 14001 Standards, have a safety management system in place.Our R&D team masters core technology for process-design of target building block
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inquiryProduct Name: 2,4,6-Tribromophenol Synonyms: BROMOL;2,4,6-TRIBROMOPHENOL;2,4,6-TRIBROMOPHENOL, 1X1ML, CH2CL2, 200 0UG/ML;2,4,6-TRIBROMOPHENOL, 1000MG, NEAT;2,4,6-TRIBROMOPHENOL, 1X1ML, MEOH, 2000U G/ML;2,4,6-TRIBROMOPHENOL OEKANAL, 250 MG;2,4,6-Tr
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inquiryWith our good experience, we offer detailed technical support and advice to assist customers. We communicate closely with customers to establish their quality requirements. Consistent Quality Our plant has strict quality control in each manufacturin
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inquiryWITH US,YOUR MONEY IN SAFE,YOUR BUSINESS IN SAFE 1)Quick Response Within 12 hours; 2)Quality Guarantee: All products are strictly tested by our QC, confirmed by QA and approved by third party lab in China, USA, Canada, Germany, UK, Italy, France et
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inquiryChemical Name:2,4,6-Tribromophenol CAS No.: 118-79-6 Molecular Fomula:C6H3Br3O Chemical Structure: Molecular weight: 330.8 Appearance: white granule Assay:99.5% Appearance: White powder Storage:Store in cool and dry place, away from sun light. P
Hebei Yanxi Chemical Co., Ltd. is a professional research, development and production of lead acetate benzene acetamide enterprise backbone members by local well-known entrepreneurs and professional senior engineers in the party's "low car
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inquiryAppearance:White granular Storage:ln stock Package:25kg/Barrel Application:Chemicals Transportation:Express/Sea/Air Port:Any port in china
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inquiry1.No Less 8 years exporting experience. Clients can 100% received goods 2.Lower Price with higher quality 3,Free sample 4,We are sincerely responsible for the "product quality" and "After Service" Upbio is Specialized
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inquiryProduct Name: 2,4,6-Tribromophenol CAS: 118-79-6 MF: C6H3Br3O MW: 330.8 EINECS: 204-278-6 Mol File: 118-79-6.mol 2,4,6-Tribromophenol Structure 2,4,6-Tribromophenol Chemical Properties Melting point 90-94 °C(lit.) Boiling
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inquiryOur company has been in existence for 10 years since its establishment. We have our own unique team. The company integrates independent research and development, production and sales. We have established famous brands at home and abroad. At prese
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inquiryHello, dear friend! I'm Hansen and Allen from China. Welcome to my lookchem mall! The following is a brief introduction of our company's products and services. If you are interested in our products, please contact us by emai
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inquiryMinimum Order Qty. 10 Gram Supply Ability 500 Kilograms/Month Storage store in cool, dry, ventilated place 20℃ Delivery Time 3 business days after payment Payment Term TT,western union,Paypal,MoneyGram Package 10g,20g,50g,100g,500g,1KGS,
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inquiryHenan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod
Hangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det
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inquiryCompany Introduction 1. Established in 2005, with two independent business divisions: Fine chemicals division; Pharmaceutical division. 2. Main product: Optical brightener Textile auxiliary Dye stuff Pigments
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inquiryJ&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia
Our Advantages Production: Advanced chemical equipment with years of experience Staffs for producing various extract products. Quality Control:A complete set of Testing Professional and Analysis Equipment ensures the Quality Requirements and Specif
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inquiryZibo Hangyu Biotechnology Development Co., Ltd is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemi
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inquirymoderate price & quick delivery Appearance:WHITE TO SLIGHTLY BROWN POWDER Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:100g/bottle,1kg/bottle,25kg/drum or as per your request Application:Used for preparing
Product name: 2,4,6-Tribromophenol CAS No.:118-79-6 Molecule Formula:C6H3Br3O Molecule Weight:330.80 Purity: 99.0% Package: 25kg/drum Description:White powder Manufacture Standards:Enterprise Standard TESTING ITEMS
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inquiryProduct Details Grade: pharmaceutical grade Purity:99%+ ProductionCapacity: 1000 Kilogram/Month Scope of use: For scientific research only(The product must be used legally) Our Advantage 1. Best quality with competitive price. 2. Quick shipping,
Cas:118-79-6
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inquiryOur Advantages A. International Top level TechnologyOur company owned biomedicine experts are famous at home and abroad with rich experience in research and development in the field of efficient chiral functional molecules research and development an
GMP standard, high purity, competitive price, in stock 1. Quick Response: within 6 hours after receiving your email. 2. Quality Guarantee: All products are strictly tested by our QC, confirmed by QA, and approved by a third-party lab in China, USA,
Conditions | Yield |
---|---|
With sulfuric acid; dihydrogen peroxide; acetic acid; sodium bromide at 20 - 45℃; Temperature; Reagent/catalyst; | 99% |
With tetrabutylammomium bromide; dihydrogen peroxide; vanadia In water; acetonitrile at 5℃; for 1h; Bromination; | 98% |
With tetra-N-butylammonium tribromide In water; acetonitrile at 5℃; | 98% |
Conditions | Yield |
---|---|
With benzyltrimethylammonium tribromide; calcium carbonate In methanol; dichloromethane | 99% |
With dibromamine-T In acetonitrile at 20℃; for 0.166667h; | 85% |
Multi-step reaction with 2 steps 1: bromine / acetic acid; ethanol / 1 h / 0 °C 2: 3-oxo-1,3-dihydroisobenzofuran-1-carbonitrile; lithium tert-butoxide / tetrahydrofuran / 6.5 h / -78 - 25 °C / Inert atmosphere View Scheme |
2-(3,4-methylenedioxyphenyl)-1,3-dithiane
2,4,4,6-Tetrabromo-2,5-cyclohexadien-1-one
A
piperonal
B
2,4,6-tribromophenol
Conditions | Yield |
---|---|
With dihydrogen peroxide In water; acetonitrile at 20℃; for 0.25h; | A 98% B 80% |
4-Methanesulfonyloxy-benzenesulfonic acid 2,4,6-tribromo-phenyl ester
2,4,6-tribromophenol
Conditions | Yield |
---|---|
With sodium hydride In N,N,N,N,N,N-hexamethylphosphoric triamide for 2.16667h; Ambient temperature; | 97% |
Conditions | Yield |
---|---|
With benzyltrimethylammonium tribromide; calcium carbonate In methanol; dichloromethane | 96% |
Conditions | Yield |
---|---|
With water; hydrogen bromide; Aliquat 336 at 105℃; for 5h; Catalytic behavior; | 95% |
2,4,6-tribromophenol
Conditions | Yield |
---|---|
With magnesium In tetrahydrofuran; methanol at 20℃; for 5h; | 91% |
Conditions | Yield |
---|---|
With bromine In dichloromethane at 20℃; regioselective reaction; | 90% |
Multi-step reaction with 2 steps 1: dihydrogen peroxide; water / ethanol / 0.02 h / 20 °C / Green chemistry 2: dihydrogen peroxide; hydrogen bromide; water / ethanol / 0.02 h / 20 °C / Green chemistry View Scheme |
4-Methanesulfonyl-benzenesulfonic acid 2,4,6-tribromo-phenyl ester
2,4,6-tribromophenol
Conditions | Yield |
---|---|
With sodium hydride In N,N,N,N,N,N-hexamethylphosphoric triamide for 2.16667h; Ambient temperature; | 89% |
C6H5Br3O
2,4,6-tribromophenol
Conditions | Yield |
---|---|
With oxygen; copper diacetate; trifluoroacetic acid; lithium bromide In acetonitrile at 80℃; under 760.051 Torr; for 10h; Sealed tube; | 89% |
di(p-tolyl) disulfide
para-thiocresol
4-Methanesulfonyloxy-benzenesulfonic acid 2,4,6-tribromo-phenyl ester
A
tris(p-tolylthio)methane
B
2,4,6-tribromophenol
Conditions | Yield |
---|---|
With sodium hydride In N,N,N,N,N,N-hexamethylphosphoric triamide for 2.16667h; Ambient temperature; | A 22% B 87% |
Conditions | Yield |
---|---|
With trans-3,5-dihydroperoxy-3,5-dimethyl-1,2-dioxolane; hydrogen bromide In water at 20℃; for 1.6h; | 86% |
With trans-3,5-dihydroperoxy-3,5-dimethyl-1,2-dioxolane; ammonium bromide; acetic acid at 20℃; for 2h; regioselective reaction; | 85% |
Conditions | Yield |
---|---|
With water; hydrogen bromide; dihydrogen peroxide In ethanol at 20℃; for 0.0166667h; Green chemistry; | 84% |
phenol
A
4-bromo-phenol
B
2-hydroxybromobenzene
C
2,4,6-tribromophenol
Conditions | Yield |
---|---|
With pyridine; bromine; silver nitrate In acetonitrile for 2h; Ambient temperature; | A 3% B 82% C 3% |
With N-Bromosuccinimide In acetonitrile at 20℃; for 0.166667h; | A 12 %Chromat. B 7 %Chromat. C 55 %Chromat. |
(2,4,6-tribromo-phenoxy)-acetic acid
2,4,6-tribromophenol
Conditions | Yield |
---|---|
Stage #1: (2,4,6-tribromo-phenoxy)-acetic acid With triethylamine In N,N-dimethyl-formamide; toluene for 3h; Curtius rearrangement; Heating; Stage #2: With potassium hydroxide In N,N-dimethyl-formamide; toluene at 25℃; for 0.133333h; Stage #3: With potassium hydroxide; glycerol In ethanol; N,N-dimethyl-formamide; toluene for 2h; Heating; Further stages.; | 82% |
Conditions | Yield |
---|---|
With N-Bromosuccinimide; diisopropylamine In dichloromethane for 1h; Ambient temperature; | A 80% B 5.7 % Chromat. |
di-isopropyl azodicarboxylate
2,6-dibromophenol
A
bis(1-methylethyl) 1,2-hydrazinedicarboxylate
B
2,4,6-tribromophenol
Conditions | Yield |
---|---|
With ZrBr4 In dichloromethane at 20℃; for 2h; | A n/a B 79% |
di(p-tolyl) disulfide
para-thiocresol
4-Methanesulfonyl-benzenesulfonic acid 2,4,6-tribromo-phenyl ester
A
tris(p-tolylthio)methane
B
2,4,6-tribromophenol
Conditions | Yield |
---|---|
With sodium hydride In N,N,N,N,N,N-hexamethylphosphoric triamide for 2.16667h; Ambient temperature; | A 4% B 78% |
3,7-dimethyl-2E,6-octadien-1-yl acetate
A
6-bromo-3,7-dimethylocta-2,7-dienyl acetate
B
(E)-6,7-dibromo-3,7-dimethyloct-2-en-1-yl acetate
C
8-bromo-3,7-dimethylocta-2,7-dienyl acetate
D
2,4,6-tribromophenol
Conditions | Yield |
---|---|
With 2,4,4,6-Tetrabromo-2,5-cyclohexadien-1-one In dichloromethane for 15h; Ambient temperature; Title compound not separated from byproducts; | A n/a B 14% C n/a D 76% |
2,4,4,6-Tetrabromo-2,5-cyclohexadien-1-one
A
6-bromo-3,7-dimethylocta-2,7-dienyl acetate
B
(E)-6,7-dibromo-3,7-dimethyloct-2-en-1-yl acetate
C
8-bromo-3,7-dimethylocta-2,7-dienyl acetate
D
2,4,6-tribromophenol
Conditions | Yield |
---|---|
With methyl geranate In dichloromethane for 15h; Ambient temperature; | A n/a B 14% C n/a D 76% |
2,4-dibromophenol
di-isopropyl azodicarboxylate
A
bis(1-methylethyl) 1,2-hydrazinedicarboxylate
B
2,4,6-tribromophenol
Conditions | Yield |
---|---|
With ZrBr4 In dichloromethane at 20℃; for 4h; | A n/a B 75% |
2,4,4,6-Tetrabromo-2,5-cyclohexadien-1-one
2,4,6-tribromophenol
Conditions | Yield |
---|---|
With betaine In ethanol at 60℃; for 72h; | 71.4% |
With 3-oxo-1,3-dihydroisobenzofuran-1-carbonitrile; lithium tert-butoxide In tetrahydrofuran at -78 - 25℃; for 6.5h; Inert atmosphere; | 36% |
With ammonium hydroxide; benzene |
Conditions | Yield |
---|---|
With samarium; copper(l) iodide; potassium iodide In tetrahydrofuran at 20℃; Molecular sieve; diastereoselective reaction; | A 70% B n/a |
(2-bromophenyl)boronic acid
2,4,6-tribromophenol
Conditions | Yield |
---|---|
With water; hydrogen bromide; dihydrogen peroxide In ethanol at 20℃; for 0.0166667h; Green chemistry; | 55% |
phenol
A
4-bromo-phenol
B
2,4-dibromophenol
C
2,4,6-tribromophenol
Conditions | Yield |
---|---|
With hydrogenchloride; C20H17N5O4V(1+)*ClO4(1-); dihydrogen peroxide; potassium bromide In water; acetonitrile at 20℃; for 20h; pH=3; | A 5% B 51% C 2% |
With [oxovanadium(V)(pyridine-2,6-dicarboxylate)(benzohydroxamate)]; dihydrogen peroxide; nitric acid; potassium bromide In water; acetonitrile pH=3; Reagent/catalyst; Overall yield = 72 %; | A 11% B 41% C 12% |
With hydrogenchloride; dihydrogen peroxide; potassium bromide In water; acetonitrile at 20℃; for 20h; pH=Ca. 3; | A 13% B 27% C 41% |
Conditions | Yield |
---|---|
With bromine for 4h; Phase-vanishing reaction with phase screen; Neat (no solvent); | A 41% B 46% |
With tetra-N-butylammonium tribromide In water; tert-butyl alcohol at 23℃; for 72h; pH=1; | A 13 %Spectr. B 86 %Spectr. |
5-bromo-2-geranyl-1,4-benzenediol
A
1,3,5-tribromo-2-methoxymethoxybenzene
C
2,4,6-tribromophenol
Conditions | Yield |
---|---|
A 16% B 35% C 42% |
Conditions | Yield |
---|---|
With dibromamine-T In acetonitrile at 20℃; | A 40% B 10% |
With bromine In water; tert-butyl alcohol at 23℃; for 72h; pH=1; | A 8 %Spectr. B 88 %Spectr. |
2,4,6-tribromoaniline
copper(I) cyanide
A
1,3,5-trisbromobenzene
B
1,2,3,5-tetrabromobenzene
C
2,4,6-tribromonitrobenzene
D
2,4,6-tribromobenzonitrile
E
2,4,6-tribromophenol
Conditions | Yield |
---|---|
With tert.-butylnitrite In dimethyl sulfoxide at 60℃; for 1.5h; Product distribution; Mechanism; other anilines; | A 37% B 7% C 4% D 20% E 4% |
2,4,6-tribromoaniline
copper(I) cyanide
A
1,3,5-trisbromobenzene
B
2,4,6-tribromonitrobenzene
C
2,4,6-tribromobenzonitrile
D
2,4,6-tribromophenol
Conditions | Yield |
---|---|
With tert.-butylnitrite In dimethyl sulfoxide at 60℃; for 1.5h; Further byproducts given; | A 37% B 4% C 20% D 4% |
2,4,6-tribromophenol
4-diisopropylsilanyl-benzoic acid 2,4,6-tribromo-phenyl ester
Conditions | Yield |
---|---|
With bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride In pyridine at 20℃; for 0.5h; | 100% |
Conditions | Yield |
---|---|
With tribenzylamine In benzene for 0.166667h; | 99.8% |
1,3,5-trichloro-2,4,6-triazine
2,4,6-tribromophenol
phenol
2,4,6-tris(2,4,6-tribromophenoxy)-1,3,5-triazine
Conditions | Yield |
---|---|
With sodium hydroxide; hydrogen bromide; bromine; hydrazine In water; acetone | 99% |
tert.-butylhydroperoxide
tri(p-tolyl)antimony
2,4,6-tribromophenol
benzene
Conditions | Yield |
---|---|
Stage #1: tert.-butylhydroperoxide; tri(p-tolyl)antimony; 2,4,6-tribromophenol In diethyl ether at 20℃; for 24h; Stage #2: benzene In n-heptane | 99% |
2,4,6-tribromophenol
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 60℃; for 18h; Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
Stage #1: 2-chloro-ethanol With tetrachlorosilane In 1,4-dioxane at 0 - 50℃; for 2h; Inert atmosphere; Stage #2: 2,4,6-tribromophenol In 1,4-dioxane at 80℃; for 5h; Stage #3: 2-chloro-ethanol In 1,4-dioxane at 25 - 50℃; for 4.5h; Solvent; Temperature; | 98.8% |
Conditions | Yield |
---|---|
Stage #1: 2,3-Dichloro-1-propanol With tetrachlorosilane In diethylene glycol dimethyl ether at 8 - 35℃; for 2h; Inert atmosphere; Stage #2: 2,4,6-tribromophenol In diethylene glycol dimethyl ether at 90℃; for 4h; Inert atmosphere; Stage #3: 2,3-Dichloro-1-propanol In diethylene glycol dimethyl ether at 50 - 95℃; for 5h; Temperature; Solvent; Inert atmosphere; | 98.6% |
4-bromophenyl butyl ether
2,4,6-tribromophenol
1,3,5-tribromo-2-phenoxybutoxybenzene
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 70℃; for 17h; | 98.5% |
1-Bromooctadecane
2,4,6-tribromophenol
1,3,5-tribromo-2-octadecyloxybenzene
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 70℃; for 17h; | 98.5% |
Conditions | Yield |
---|---|
In diethyl ether; water aq. H2O2 was added to mixt. of SbPh3 and ligand in ether, allowed to stand for 12 h; solvent was evapd., washed with benzene, dried; | 98% |
1,3,5-trichloro-2,4,6-triazine
2,4,6-tribromophenol
2,4,6-tris(2,4,6-tribromophenoxy)-1,3,5-triazine
Conditions | Yield |
---|---|
With magnesium silicate; sodium hydroxide; sodium sulfite; trimethylamine In dichloromethane; water at 3 - 30℃; Product distribution / selectivity; Reflux; | 98% |
Stage #1: 2,4,6-tribromophenol With potassium carbonate In acetone for 1.5h; Heating / reflux; Stage #2: 1,3,5-trichloro-2,4,6-triazine In acetone at 25℃; for 3.25h; Heating / reflux; |
ethyl 5-bromovalerate
2,4,6-tribromophenol
ethyl 5-(2,4,6-tribromophenoxy)pentanoate
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 50℃; for 24h; | 98% |
With potassium carbonate In N,N-dimethyl-formamide at 50℃; for 12h; Inert atmosphere; | 88% |
Conditions | Yield |
---|---|
Stage #1: 1,3-Dichloro-2-propanol With tetrachlorosilane In 1,1,2,2-tetrachloroethane at 8 - 35℃; for 2h; Inert atmosphere; Stage #2: 2,4,6-tribromophenol In 1,1,2,2-tetrachloroethane at 85℃; for 4.5h; Inert atmosphere; Stage #3: 1,3-Dichloro-2-propanol In 1,1,2,2-tetrachloroethane at 50 - 90℃; for 5.5h; Solvent; Temperature; Inert atmosphere; | 98% |
1-methyl-1H-imidazole
1,3,5-trichloro-2,4,6-triazine
2,4,6-tribromophenol
2,4,6-tris(2,4,6-tribromophenoxy)-1,3,5-triazine
Conditions | Yield |
---|---|
Stage #1: 1-methyl-1H-imidazole; 2,4,6-tribromophenol In chlorobenzene at 40℃; for 2h; Stage #2: 1,3,5-trichloro-2,4,6-triazine In chlorobenzene at 20 - 25℃; for 4h; Temperature; | 98% |
Conditions | Yield |
---|---|
Stage #1: 2-bromoethanol With tetrachlorosilane In diethylene glycol dimethyl ether at 0 - 20℃; for 2h; Inert atmosphere; Stage #2: 2,4,6-tribromophenol In diethylene glycol dimethyl ether at 60℃; for 5h; Stage #3: 2-bromoethanol In diethylene glycol dimethyl ether at 25 - 45℃; for 5.5h; Solvent; Temperature; | 97.3% |
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide Heating; | 97.1% |
Conditions | Yield |
---|---|
With sodium In methanol for 7h; Heating; | 97% |
4-methoxyphenylboronic acid
2,4,6-tribromophenol
2,4,6-tris(4-methoxyphenyl)phenol
Conditions | Yield |
---|---|
With sodium carbonate; palladium diacetate In water; N,N-dimethyl-formamide at 60℃; for 12h; Suzuki; | 97% |
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 27℃; | 97% |
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 18h; | 97% |
With sodium hydride In mineral oil at 80℃; |
Conditions | Yield |
---|---|
With pyrographite In dichloromethane at 20℃; for 1.5h; Acetylation; | 96% |
With lanthanum(III) nitrate at 20℃; for 0.3h; | 95% |
With sodium acetate | |
With sodium hydroxide | |
With sulfuric acid; acetic acid |
Conditions | Yield |
---|---|
With sodium carbonate; palladium diacetate In water; N,N-dimethyl-formamide at 60℃; for 12h; Suzuki; | 96% |
With potassium fluoride; palladium diacetate for 0.166667h; Suzuki coupling reaction; microwave irradiation; | 76% |
With sodium carbonate In N,N-dimethyl-formamide at 120℃; for 6h; Suzuki-Miyaura coupling reaction; Inert atmosphere; | 62% |
With C28H40Br4N4Pd2; potassium carbonate In water; acetone at 20℃; for 24h; Suzuki Coupling; | 50% |
With tetrakis(triphenylphosphine) palladium(0); sodium carbonate at 100℃; for 0.5h; Suzuki-Miyaura Coupling; Microwave irradiation; Inert atmosphere; |
Conditions | Yield |
---|---|
With cesium fluoride In acetonitrile for 5h; Heating; | 96% |
Conditions | Yield |
---|---|
With ammonia In chloroform at 55℃; for 2h; Temperature; Concentration; Solvent; Reagent/catalyst; Inert atmosphere; Sealed tube; | 95.3% |
mononitrophenyl carbonate
2,4,6-tribromophenol
bis(2,4,6-tribromophenyl) carbonate
Conditions | Yield |
---|---|
dmap In dichloromethane at 25℃; for 8h; | 95% |
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