ChemicalBook > Product Catalog > Biochemical Engineering > Amino Acids and Derivatives > BOC-amino acid > Bromomethyl methyl ether
Bromomethyl methyl ether
Bromomethyl methyl ether Basic information
- Product Name:
- Bromomethyl methyl ether
- Synonyms:
-
- METHOXYMETHYL BROMIDE
- BROMOMETHYL METHYL ETHER
- Bromo(methoxy)methane
- bromomethoxy-methan
- Ether, bromomethyl methyl
- Methane, bromomethoxy-
- BROMOMETHYL METHYL ETHER, TECH., 90%
- BMME~Methoxymethylbromide
- CAS:
- 13057-17-5
- MF:
- C2H5BrO
- MW:
- 124.96
- Product Categories:
-
- Ethers
- Organic Building Blocks
- Oxygen Compounds
- Mol File:
- 13057-17-5.mol
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Bromomethyl methyl ether Chemical Properties
- Boiling point:
- 87 °C (lit.)
- Density
- 1.531 g/mL at 25 °C (lit.)
- refractive index
- n20/D 1.456(lit.)
- Flash point:
- 80 °F
- storage temp.
- 2-8°C
- solubility
- Chloroform (Soluble), Methanol (Slightly)
- form
- clear liquid
- Specific Gravity
- 1.531
- color
- Colorless to Light yellow to Light orange
- Water Solubility
- Sparingly soluble in water.
- Sensitive
- Moisture Sensitive
- BRN
- 1730853
- CAS DataBase Reference
- 13057-17-5(CAS DataBase Reference)
- NIST Chemistry Reference
- Bromomethyl methyl ether(13057-17-5)
- EPA Substance Registry System
- Methane, bromomethoxy- (13057-17-5)
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Safety Information
- Hazard Codes
- Xn
- Risk Statements
- 10-20/21/22-36/37/38-40
- Safety Statements
- 26-36/37
- RIDADR
- UN 1992 3/PG 3
- WGK Germany
- 3
- TSCA
- Yes
- HazardClass
- 6.1
- PackingGroup
- II
- HS Code
- 29091990
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
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Bromomethyl methyl ether Usage And Synthesis
Chemical Properties
Colorless liquid
Uses
Bromomethyl methyl ether is used as reagent for protection of OH groups as their methoxymethyl (MOM) ethers. It is used in enantiocontrolled synthesis of intermediate containing carbons 18 to 35 of the macrocyclic immunosuppressant FK-506. It was used in the synthesis of 1-methoxymethyl-4-tritylthio-2-azetidinone.
Uses
Bromomethyl methyl ether was used in enantiocontrolled synthesis of intermediate containing carbons 18 to 35 of the macrocyclic immunosuppressant FK-506. It was used in the synthesis of 1-methoxymethyl-4-tritylthio-2-azetidinone.
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