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2065-75-0

2-BROMOMALONALDEHYDE

CAS: 2065-75-0

Molecular Formula: C3H3BrO2

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2065-75-0 - Names and Identifiers

Name 2-BROMOMALONALDEHYDE
Synonyms bromopropanedial
2-Bromomaloldehyde
BROMOMALONALDEHYDE
Propanedial, bromo-
BROMOMALONALDEHYDE
2-BROMOMALONALDEHYDE
Propanedial, 2-broMo-
2-bromomalondialdehyde
2-broMo-1,3-propanedial
2-BroMo-1,3-propanedialdehyde
2-Bromomalondialdehyd for synthesis
CAS 2065-75-0
InChI InChI=1/C3H3BrO2/c4-3(1-5)2-6/h1-3H

2065-75-0 - Physico-chemical Properties

Molecular FormulaC3H3BrO2
Molar Mass150.96
Density1.750±0.06 g/cm3(Predicted)
Melting Point132-136°C(lit.)
Boling Point134.8±25.0 °C(Predicted)
Flash Point69.5°C
Solubility Acetonitrile (Slightly), DMSO (Slightly)
Vapor Presure7.95mmHg at 25°C
AppearanceBright yellow solid
ColorPale Beige to Pale Yellow
pKa1.70±0.10(Predicted)
Storage ConditionInert atmosphere,Store in freezer, under -20°C
SensitiveAir Sensitive
Refractive Index1.468
MDLMFCD00459999
UseIt is used to construct 1, 4-dihydroquinoline, whose C- 3 chiral sulfoxide group can be used as a cyclic NADH model to participate in the asymmetric reduction of methyl benzoylformate to produce phenylethyl? alkyd methyl ester. For the formation of glyoxal-derived adduct from the substituent guanine

2065-75-0 - Risk and Safety

Hazard SymbolsXi - Irritant
Irritant
Risk Codes36/37/38 - Irritating to eyes, respiratory system and skin.
Safety DescriptionS26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36 - Wear suitable protective clothing.
WGK Germany3
HS Code29130000
Hazard NoteIrritant/Keep Cold

2065-75-0 - Reference Information

overview 2-bromomalondialdehyde is a pharmaceutical intermediate, which can be prepared from 1,1,3, 3-tetramethoxypropane in one step.
Preparation 2-bromomalondialdehyde is an aldehyde compound, which can be used to prepare lometrexol intermediate 2-teramido-4-hydroxy-6-bromopyridine and [2,3-d] pyrimidine.
Use Used to construct 1, 4-dihydroquinoline, whose C- 3 chiral sulfoxide group can be used as a cyclic NADH model to participate in the asymmetric reduction reaction of methyl benzoylformate to produce phenylethyl? methyl alkyd. Used to form glyoxal-derived adducts from substituent guanine
Last Update:2024-04-09 15:16:48
2065-75-0
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