10368-81-7

Basic information

• Product Name: methyl 4-O-benzoyl-6-bromo-6-deoxyhexopyranoside
• Synonyms: methyl 4-O-benzoyl-6-bromo-6-deoxyhexopyranoside
• CAS NO: 10368-81-7
• Molecular Formula: C₁₄H₁₇BrO₆
• Molecular Weight: 361.18518
• Mol File: 10368-81-7.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: methyl 4-O-benzoyl-6-bromo-6-deoxyhexopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 4-O-benzoyl-6-bromo-6-deoxyhexopyranoside(10368-81-7)
• EPA Substance Registry System: methyl 4-O-benzoyl-6-bromo-6-deoxyhexopyranoside(10368-81-7)

Safety Data

• Hazardous Substances Data: 10368-81-7(Hazardous Substances Data)

Upstream product

• 3162-96-7 4,6-O-benzylidene-1-O-methyl-α-D-glucopyranoside 

Downstream Products

• 98405-79-9 (E)-2,2-dimethyl-4-phenylbut-3-enenitrile 
• 56543-17-0 methyl 4-O-benzoyl-6-bromo-6-deoxy-2,3-di-O-methyl-α-D-glucopyranoside 
• 79774-49-5 methyl 4-O-benzoyl-6-bromo-2,3,6-trideoxy-α-D-erythro-hex-2-enopyranoside 
• 79774-54-2 methyl 4-O-benzoyl-6-deoxy-α-D-glucopyranoside 
• 7465-44-3 methyl 6-bromo-6-deoxy-α-D-glucopyranoside 
• 81823-32-7 methyl (methyl 4-O-benzoyl-6-deoxy-2,3-di-O-methyl-α-D-gluco-heptopyranosid)uronate 
• 61243-00-3 methyl 4-O-benzoyl-2,3,6-trideoxy-α-D-erythro-hex-2-enopyranoside 
• 51785-62-7 Benzoic acid (2R,3R,4S,5R,6S)-4,5-diacetoxy-6-methoxy-2-methyl-tetrahydro-pyran-3-yl ester 
• 79774-53-1 methyl 4,6-di<(N-benzyl)methylamino>-6-bromo-2,3,4,6-tetradeoxy-α-D-erythro-hex-2-enopyranoside 
• 79774-52-0 methyl 4-<(N-benzyl)methylamino>-6-bromo-2,3,4,6-tetradeoxy-α-D-erythro-hex-2-enopyranoside 
• 101155-77-5 methyl 2,3-di-O-p-toluenesulfonyl-4-O-benzoyl-6-S-acetyl-6-thio-α-D-glucopyranoside 
• 101155-79-7 methyl 2,3-di-O-p-toluenesulfonyl-4,6-thioanhydro-α-D-gulopyranoside 
• 101155-80-0 Toluene-4-sulfonic acid (1R,3S,4R,5S,6R)-5-hydroxy-3-methoxy-7,7-dioxo-2-oxa-7λ⁶-thia-bicyclo[4.2.0]oct-4-yl ester 
• 101155-78-6 methyl 2-O-p-toluenesulfonyl-4,6-thioanhydro-α-D-gulopyranoside 

Relevant articles and documents

Substituted benzyl ethers as radical stable protecting groups

Sixteen substituted benzyl ethers were studied for their potential to serve as hydroxyl protecting groups with the ability to withstand radical brominating conditions using N-bromosuccinimide during the conversion of benzylidene 2 into bromobenzoate 3.