ChemicalBook > CAS DataBase List > 1-(TERT-BUTOXYCARBONYL)-5-METHYLINDOLE&
1-(TERT-BUTOXYCARBONYL)-5-METHYLINDOLE&
1-(TERT-BUTOXYCARBONYL)-5-METHYLINDOLE&
- CAS No.129822-49-7
- Chemical Name:1-(TERT-BUTOXYCARBONYL)-5-METHYLINDOLE&
- CBNumber:CB3500127
- Molecular Formula:C14H17NO2
- Formula Weight:231.29
- MOL File:129822-49-7.mol
1-(TERT-BUTOXYCARBONYL)-5-METHYLINDOLE& Property
- Boiling point 208-209 °C(lit.)
- Density 1.056 g/mL at 25 °C(lit.)
- refractive index n
20/D 1.5410(lit.) - Flash point >230 °F
- form solid
- UNSPSC Code 12352100
- NACRES NA.22
Safety
-
Symbol(GHS)
- Signal wordDanger
- Hazard statements H301-H317
- Precautionary statements P280-P301+P310
1-(TERT-BUTOXYCARBONYL)-5-METHYLINDOLE& Price
More Price(1)
- Brand: Sigma-Aldrich(India)
- Product number: 636479
- Product name : 1-(tert-Butoxycarbonyl)-5-methylindole
- Purity: 97%
- Packaging: 5G
- Price: ₹25568.65
- Updated: 2022/06/14
- Buy: Buy
1-(TERT-BUTOXYCARBONYL)-5-METHYLINDOLE& Chemical Properties,Usage,Production
- Uses Reactant in stereoselective preparation of substituted dihydroindole derivatives via palladium-catalyzed stereoselective carboaminoxylation reactions Reactant in conversion of 1-Boc-indoles to 1-Boc-oxindoles Reactant in preparation of indolyl aromatic chiral alpha-sulfoxides Reactant in preparation of (indolyl)borates, silanes, and silanols.
-
Uses
- Reactant in stereoselective preparation of substituted dihydroindole derivatives via palladium-catalyzed stereoselective carboaminoxylation reactions
- Reactant in conversion of 1-Boc-indoles to 1-Boc-oxindoles
- Reactant in preparation of indolyl aromatic chiral alpha-sulfoxides
- Reactant in preparation of (indolyl)borates, silanes, and silanols
1-(TERT-BUTOXYCARBONYL)-5-METHYLINDOLE& Preparation Products And Raw materials
Raw materials
Preparation Products
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129822-49-7, 1-(TERT-BUTOXYCARBONYL)-5-METHYLINDOLE&Related Search:
- 1-BOC-5-METHYL-1H-INDOLE-2-BORONIC ACID 1-Boc-5-Cyanoindole-2-boronic acid 5-CYANO-3-IODOINDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER 1-BOC-5-CYANOINDOLE N-BOC-1H-INDOLE-5-CARBALDEHYDE 3-BROMO-5-CYANOINDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER 1-BOC-2-DIMETHYLSILANYL-5-METHYL-INDOLE 1-(TERT-BUTYL) 5-METHYL 3-(2-AMINOETHYL)-1H-INDOLE-1,5-DICARBOXYLATE HYDROCHLORIDE 1-BOC-2-(HYDROXY-DIMETHYL-SILANYL)-5-METHYL-INDOLE 5-aminomethyl-indole-1-carboylic acid tert-butyl ester 1-(TERT-BUTOXYCARBONYL)-5-METHYLINDOLE& 5-CYANO-3-HYDROXYMETHYLINDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER N-TERT-BUTOXYCARBONYL-1-METHOXY-3-(METHOXYCARBONYL) CARBAZOLE 3-HYDROXYMETHYL-5-METHYLINDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER 3-BROMO-5-METHYLINDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER 3-IODO-5-METHYLINDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER TERT-BUTYL5-([4-(TERT-BUTOXYCARBONYL)-PIPERAZIN-1-YL]-METHYL)-1H-INDOLE-1-CARBOXYLATE 5-METHYL-3-FORMYLINDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
- Indoles
- Heterocyclic Compounds
- Heterocyclic Building Blocks
- Building Blocks
- 杂环化合物
- 5-甲基-1H-吲哚-1-羧酸叔丁酯
- 1-(叔丁氧羰基)-5-甲基吲哚
- 1-(叔丁氧基羰基)-5-甲基吲哚
- 129822-49-7
- 1-(<i>tert</i>-Butoxycarbonyl)-5-methylindole
- 1,1-Dimethylethyl 5-methyl-1H-indole-1-carboxylate
- 1-BOC-5-methylindole
- 1-(tert-Butoxycarbonyl)-5-methylindole 97%
- 1H-Indole-1-carboxylic acid, 5-methyl-, 1,1-dimethylethyl ester
- tert-Butyl 5-methylindole-1-carboxylate
- tert-Butyl 5-Methyl-1H-indole-1-carboxylate