- Bredereck's reagent
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- $11.00 / 25g
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2024-04-12
- CAS:5815-08-7
- Min. Order: 25g
- Purity: 0.90
- Supply Ability: 200kg
- BREDERECK'S REAGENT
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- $1.10 / 1g
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2022-08-19
- CAS:5815-08-7
- Min. Order: 1g
- Purity: 99.00%
- Supply Ability: 100 Tons Min
- BREDERECK"S REAGENT
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- $15.00 / 1KG
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2021-08-11
- CAS:5815-08-7
- Min. Order: 1KG
- Purity: 99%+ HPLC
- Supply Ability: Monthly supply of 1 ton
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| BREDERECK'S REAGENT Basic information |
Product Name: | BREDERECK'S REAGENT | Synonyms: | tert-Butoxy bis(dimethylamino)methane technical;BREDERECKS REAGENT;BREDERECK'S REAGENT;tert-Butoxybis(dimethylamino)methane, 85+%;Bis(dimethylamino)(tert-butoxy)methane;N,N,N',N'-Tetramethyl(tert-butoxy)methanediamine;N,N,N',N'-Tetramethyl-α-tert-butoxymethanediamine;α-(1,1-Dimethylethoxy)-N,N,N',N'-tetramethylmethanediamine | CAS: | 5815-08-7 | MF: | C9H22N2O | MW: | 174.28 | EINECS: | 227-383-9 | Product Categories: | Building Blocks;Chemical Synthesis;Nitrogen Compounds;Organic Building Blocks;Polyamines;Elisa Kit-plant ELISA Kit | Mol File: | 5815-08-7.mol | |
| BREDERECK'S REAGENT Chemical Properties |
Boiling point | 50-55 °C/15 mmHg (lit.) | density | 0.844 g/mL at 25 °C (lit.) | refractive index | n20/D 1.422(lit.) | Fp | 106 °F | storage temp. | Sealed in dry,Store in freezer, under -20°C | solubility | Chloroform (Sparingly), DMSO (Sparingly), Methanol (Slightly) | pka | 5.46±0.38(Predicted) | form | Liquid | color | Clear pale yellow | Specific Gravity | 0.844 | BRN | 1901973 | Stability: | Hygroscopic | InChI | InChI=1S/C9H22N2O/c1-9(2,3)12-8(10(4)5)11(6)7/h8H,1-7H3 | InChIKey | HXRAMSFGUAOAJR-UHFFFAOYSA-N | SMILES | C(OC(C)(C)C)(N(C)C)N(C)C | CAS DataBase Reference | 5815-08-7(CAS DataBase Reference) |
Hazard Codes | Xi,F | Risk Statements | 10-36/37/38 | Safety Statements | 26 | RIDADR | UN 1993 3/PG 3 | WGK Germany | 3 | F | 10 | HazardClass | 3 | PackingGroup | III | HS Code | 29221990 |
| BREDERECK'S REAGENT Usage And Synthesis |
Chemical Properties | Clear pale yellow liquid | Uses | Reactant for:
- Preparation of pyrroloquinazolines as photochemotherapeutic agents
- Enanatioslective formal synthesis of the Cinchona alkaloid quinine via stereoselective intermolecular radical addition
- Synthesis of camptothecin via intramolecular isomuenchnone cycloaddition reaction
- Aminomethylenation reactions
| Uses | Mild enamination reagent; catalyst in ring-opening polymerization reactions. | Uses | Reactant for:• ;Preparation of pyrroloquinazolines as photochemotherapeutic agents1• ;Enanatioslective formal synthesis of the Cinchona alkaloid quinine via stereoselective intermolecular radical addition2• ;Synthesis of camptothecin via intramolecular isomuenchnone cycloaddition reaction3• ;Aminomethylenation reactions4 |
| BREDERECK'S REAGENT Preparation Products And Raw materials |
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