CAS 2032-35-1
:Acétal diéthylique de bromoacétaldéhyde
- 2-Bromo-1,1-diethoxyethane
- Bromoacetal
- Bromoacetal dehyde diethyl acetal
- Bromoacetaldehydediethylacetal
- Bromo acetaldehyde diethyl acetal
- Bromoacetaldehyde diethyl acetal
- 1,1-Diethoxy-2-bromoethane
- 1-Bromo-2,2-diethoxyethane
- 2,2-Diethoxyethyl bromide
- 2-Brom-1,1-diethoxyethan
- 2-Bromo-1,1-Dietoxietano
- 2-Bromoacetaldehyde diethyl acetal
- Acetaldehyde, bromo-, diethyl acetal
- Bromacetal
- Bromacetaldehyde diethyl acetal
- Diethyl bromoacetaldehyde acetal
- Ethane, 2-bromo-1,1-diethoxy-
- Nsc 8036
- Voir plus de synonymes
Bromoacetaldehyde diethyl acetal, 97%
CAS :Bromoacetaldehyde diethyl acetal, is used as a synthetic building block. It is mainly used for synthesis of antibiotics such as erythromycin and cephalosporins and to other drugs. It also can be used as pharmaceutical intermediates. Besides, this chemical can be used to pruduce drugs such as methylt
Formule :C6H13BrO2Degré de pureté :97%Couleur et forme :Clear colorless to pale yellow, LiquidMasse moléculaire :197.07Ethane, 2-bromo-1,1-diethoxy-
CAS :Formule :C6H13BrO2Degré de pureté :98%Couleur et forme :LiquidMasse moléculaire :197.0702Bromoacetaldehyde diethyl acetal
CAS :Bromoacetaldehyde diethyl acetalFormule :C6H13BrO2Degré de pureté :97%Couleur et forme : colourless liquidMasse moléculaire :197.07g/molBromoacetaldehyde Diethyl Acetal
CAS :Formule :C6H13BrO2Degré de pureté :>95.0%(GC)Couleur et forme :Colorless to Light yellow clear liquidMasse moléculaire :197.07Bromoacetaldehyde diethyl acetal
CAS :Formule :C6H13BrO2Degré de pureté :97.0%Couleur et forme :Liquid, OilMasse moléculaire :197.072Bromoacetaldehyde Diethyl Acetal
CAS :Produit contrôléApplications Bromoacetaldehyde Diethyl Acetal (cas# 2032-35-1) is a compound useful in organic synthesis.
Formule :C6H13BrO2Couleur et forme :NeatMasse moléculaire :197.07Bromoacetaldehyde diethyl acetal
CAS :Bromoacetaldehyde diethyl acetal (BDAE) is an organic compound that has been shown to have receptor binding activity. BDAE binds to the ethylene diamine receptor and competes with ethylene diamine for binding sites. It also forms acid from sodium carbonate and hydrochloric acid, which may be due to its ability to act as a solid catalyst. BDAE has shown activity in hiv infection, with a potency comparable to that of dimethyl fumarate. The synthesis of BDAE can be accomplished by reacting monosodium malonate ester hydrochloride with adenine nucleotide and malonic acid. The reaction solution is heated until the desired product crystallizes out of solution.
Formule :C6H13BrO2Degré de pureté :Min. 95%Masse moléculaire :197.07 g/mol







