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1H-2,1,3-Benzothiadiazin-4(3H)-one, 3-(1-methylethyl)-, 2,2-dioxide

Sharpless, Asymmetric Dihydroxylation (AD)/Cyclization of N-DiBoc Allylic and Homoallylic Amines: Selective Differentiation of the Hydroxyl Groups, , 34, 5545 (1993).

Zargarian, Synthesis of Optically Active Secondary Allylic Alcohols from Allylsilanes via Successive Asymmetric Dihydroxylation (AD) and Peterson Olefination Reactions, , 34, 2509 (1993

Yield: 27% Charge a RBF with 0.05 mmol Pd(OAc)2, 1 mmol of methyl 4-nitrobenzoate, and 5 mL of THF.

Phenol, 2-(2H-benzotriazol-2-yl)-4,6-bis(1,1-dimethylpropyl)-

L-Ascorbic acid, 2-[(2R)-3,4-dihydro-2,5,7,8-tetramethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]-2H-1-benzopyran-6-YL hydrogen phosphate], potassium salt (1:1)

Sharpless, Enantioselective Synthesis of Both Enantiomers of 7,7-Dimethyl-6,8-dioxabicyclo-[3.2.1]octane via Regioselective Asymmetric Dihydroxylation, , 1, 47 (1993) .

1,4-Cyclohexanedimethanol, dibenzoate

The traditional metal based oxidising reagents are replaced by iodosobenzoates due to their outstanding reactivity, selectivity and environment management.

H. Wu, et al. Methyl 4-nitro­benzoate.Acta Cryst.,2009,E653096.Peter. J. Groenewegen. Novel degradative pathway of 4-nitrobenzoate in Comamonas acidovorans NBA-10.Journal of’ General Microbiolog.,1992,1381599-1605.

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Initial Removal of the 4a-Methyl Group,


2-Benzothiazolesulfenamide, N-(1,1-dimethylethyl)-

Fall 2010 24.5 mg of 4-Nitrobenzoic acid was stirred in about 2.655 mL of methanol.
0.19 mL of thionyl chloride was added to the solution drop wise under 10 degrees Celsius.
Reaction must stir under ice bath for 3 hours.
After the reaction is stirred methanol is distilled out.
About 4.3 mL of water was added to the mixture.
Then the mixture was extraced with ethyl acetate and washed with saturated sodium bicarbonate.
The solution was then placed in a rotavap, and the solid product was characterized.

Phenol, 2-(2H-benzotriazol-2-yl)-4-(1,1,3,3-tetramethylbutyl)-

Whereas the Minister of the Environment and the Minister of Health (the ministers) have assessed information in respect of the substance Clarified oils (petroleum), catalytic cracked, reaction products with cresol and poly-methylene polyphenylene isocyanate, Chemical Abstracts Service Registry No. 68920-56-9, under section 83 of the Canadian Environmental Protection Act, 1999;

Phenol, 2-(2H-benzotriazol-2-yl)-4,6-bis(1,1-dimethylethyl)-

Substances included in Part 4 of Schedule 1 are currently on the revised In Commerce List (ICL). The scope of the information being collected on these substances is limited to Food and Drugs Act–related activities, such as therapeutic products (including human and veterinary drugs, and medical devices), natural health products, foods (including food additives) and cosmetics. Substances in Part 4 of Schedule 1 that are imported or manufactured with respect to use patterns beyond the scope of the Food and Drugs Act are subject to notification requirements under the New Substances Notification Regulations of the Canadian Environmental Protection Act, 1999 (hereinafter referred to as the “Act”).

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