91352-76-0

Basic information

• Product Name: Benzene, 1-(diMethoxyMethyl)-2,4-diMethoxy-
• Synonyms: Benzene, 1-(diMethoxyMethyl)-2,4-diMethoxy-
• CAS NO: 91352-76-0
• Molecular Formula: C₁₁H₁₆O₄
• Molecular Weight: 212.24234
• Mol File: 91352-76-0.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Benzene, 1-(diMethoxyMethyl)-2,4-diMethoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-(diMethoxyMethyl)-2,4-diMethoxy-(91352-76-0)
• EPA Substance Registry System: Benzene, 1-(diMethoxyMethyl)-2,4-diMethoxy-(91352-76-0)

Safety Data

• Hazardous Substances Data: 91352-76-0(Hazardous Substances Data)

Upstream product

• 613-45-6 2,4-Dimethoxybenzaldehyde 
• 149-73-5 trimethyl orthoformate 
• 67-56-1 methanol 

Downstream Products

• 124609-25-2 2,6-dimethoxy-3-(dimethoxymethyl)-1-<(1-hydroxycyclohexyl)methyl>benzene 
• 124609-18-3 3-(cyclohex-1-en-1-ylmethyl)-2,4-dimethoxybenzaldehyde 
• 124665-41-4 C₄₀H₅₉NO₆Si 
• 613-45-6 2,4-Dimethoxybenzaldehyde 
• 343868-88-2 (3aR,8aS)-3-Benzoyl-2-(2,4-dimethoxy-phenyl)-2,3,3a,8-tetrahydro-indeno[1,2-d]oxazole-8a-carboxylic acid 
• 1026039-16-6 1-benzoyl-2-(2,4-dimethoxy-phenyl)-1,4,5,9b-tetrahydro-2H-naphtho[1,2-d]oxazole-3a-carboxylic acid 
• 124609-26-3 3-(1-hydroxycyclohex-1-yl)methyl-2,4-dimethoxybenzaldehyde 
• 124609-29-6 3-Cyclohex-1-enylmethyl-2,4-dimethoxy-benzoic acid 
• 124609-22-9 1-[5-(4,4-Dimethyl-4,5-dihydro-oxazol-2-yl)-2-methoxy-benzyl]-cyclohexanol 
• 124609-28-5 3-(cyclohex-1-en-1-ylmethyl)-2,4-dimethoxy-1-benzene 
• 124609-19-4 3-(cyclohex-1-en-1-ylmethyl)-2,4-dimethoxy-1-(4,5-dihydro-4',4'-dimethyloxazol-2'-yl)benzene 
• 124609-20-7 2-[2,4-Dimethoxy-3-(7-oxa-bicyclo[4.1.0]hept-1-ylmethyl)-phenyl]-4,4-dimethyl-4,5-dihydro-oxazole 
• 124609-21-8 3-(1-hydroxycyclohexan-1-yl)methyl-2,4-dimethoxy-1-(4,5-dihydro-4,4-dimethyloxazol-2-yl)benzene 

Relevant articles and documents

Ru(II)-functionalized SBA-15 as highly chemoselective, acid free and sustainable heterogeneous catalyst for acetalization of aldehydes and ketones

Combining electron deficient Ru(II) coordination sites with organofunctionalized SBA-15, (L)Ru(II)@SBA-15, result in a mild, neutral, water scavenger free and chemo-selective acetalization catalyst for cyclic/acyclic acetals. Vacant coordination sites of ruthenium in (L)Ru(II)@SBA-15 activates protecting groups as well as reactants simultaneously and restricts the reverse acetalization reaction. Synthesized (L)Ru(II)@SBA-15 catalyst has been thoroughly characterized and act as competitive catalyst compared to conventional acid catalysts. (L)Ru(II)@SBA-15 performs high catalytic activity as well as selectivity within 20 min with high TOF. The catalyst can be recycled and reaction parameters are optimized.

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The C-2 methylated 2S,3R and 2R,3S side chains of docetaxel have been enantioselectively prepared and esterified with protected 10-deacetylbaccatin III to provide novel analogues of docetaxel.

Tremorgenic indole alkaloid studies. 6. Preparation of an advanced intermediate for the synthesis of penitrem D. Synthesis of an indole-oxocane

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