Conditions | Yield |
---|---|
With bromine In tetrachloromethane at 0℃; Cooling with ice; | 80% |
With bromine Ambient temperature; competitive bromination with 1-heptene; other unsaturated carbonyl compound; | |
With bromine |
2,3-dibromo-propionyl chloride
2,3-dibromopropanal
Conditions | Yield |
---|---|
With lithium tri(t-butoxy)aluminum hydride In tetrahydrofuran Reduction; | 79% |
Conditions | Yield |
---|---|
bei der Ozonspaltung; |
Conditions | Yield |
---|---|
With water; bromine |
Conditions | Yield |
---|---|
With bromine |
4,5-dibromo-pent-2-enoic acid
chloroform
water
ozone
A
2,3-dibromopropanal
2,3-dibromopropanal
N-(1-trifluoromethyltrifluoroethylidene)-2-trifluoromethyl-3,3,3-trifluoropropionamide
2-(1,2-dibromoethyl)-4,4-bis(trifluoromethyl)-6-(2-hydrohexafluoroisopropyl)-2H,4H-1,3,5-dioxazine
Conditions | Yield |
---|---|
In tetrachloromethane at 100℃; for 1h; | 94.8% |
2,3-dibromopropanal
meso-2,3-Dimercaptobernsteinsaeure-dimethylester
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid | 90% |
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 20℃; for 20h; | 76% |
2,3-dibromopropanal
trimethyleneglycol
2-(1,2-dibromoethyl)-1,3-dioxane
Conditions | Yield |
---|---|
With cationite KU-2-8 In benzene Heating; | 71% |
With potassium carbonate; toluene-4-sulfonic acid 1.0 CH2Cl2, reflux, 5 h, 2.) heating.; Multistep reaction; |
2,3-dibromopropanal
ethylene glycol
2-(1',2'-dibromoethyl)-1,3-dioxolane
Conditions | Yield |
---|---|
With cationite KU-2-8 In benzene Heating; | 71% |
Conditions | Yield |
---|---|
With cationite KU-2-8 In benzene Heating; | 64% |
diazomethane
diethyl ether
2,3-dibromopropanal
3,4-dibromobutan-2-one
diazomethane
2,3-dibromopropanal
3,4-dibromobutan-2-one
Conditions | Yield |
---|---|
With diethyl ether |
Conditions | Yield |
---|---|
und Behandeln des erhaltenen Reaktionsprodukts mit 2,5,6-Triamino-3H-pyrimidin-4-on und KI; |
methanol
2,3-dibromopropanal
formimidomethylester hydrochloride
1,2-dibromo-3,3-dimethoxypropane
4,5,6-triamino-1H-pyrimidine-2-thione
2,3-dibromopropanal
N-(4-aminobenzoyl)-L-glutamic acid
N-{4-[(4-amino-2-thioxo-1,2-dihydro-pteridin-6-ylmethyl)-amino]-benzoyl}-L-glutamic acid
4,5,6-triamino-1H-pyrimidine-2-thione
2,3-dibromopropanal
4-amino-benzoic acid
4-[(4-amino-2-thioxo-1,2-dihydro-pteridin-6-ylmethyl)-amino]-benzoic acid
5,6-diaminouracil
2,3-dibromopropanal
N-(4-aminobenzoyl)-L-glutamic acid
N-{4-[(2,4-dioxo-1,2,3,4-tetrahydro-pteridin-6-ylmethyl)-amino]-benzoyl}-L-glutamic acid
Conditions | Yield |
---|---|
With sodium acetate; acetic acid |
N-(4-aminobenzoyl)-B-alanine
2,5,6-triamino-3,4-dihydro-4-pyrimidinone
2,3-dibromopropanal
N-pteroyl-β-alanine
Conditions | Yield |
---|---|
With sodium dichromate | |
With iodine |
2,5,6-triamino-3,4-dihydro-4-pyrimidinone
2,3-dibromopropanal
N-methyl-p-aminobenzoic acid
10-methyl-pteroic acid
2,5,6-triamino-3,4-dihydro-4-pyrimidinone
2,3-dibromopropanal
4-(N-butylamino)benzoic acid
2,5,6-triamino-3,4-dihydro-4-pyrimidinone
2,3-dibromopropanal
N-(4-amino-benzoyl)-alanine
Conditions | Yield |
---|---|
With sodium dichromate | |
With iodine |
2,5,6-triamino-3,4-dihydro-4-pyrimidinone
2,3-dibromopropanal
p-(N-methylamino)benzoyl-L-glutamic acid
N10-methylfolic acid
2,5,6-triamino-3,4-dihydro-4-pyrimidinone
2,3-dibromopropanal
N-(4-amino-3-methyl-benzoyl)-L-glutamic acid
N-(4-aminobenzoyl)-glutamic acid
2,5,6-triamino-3,4-dihydro-4-pyrimidinone
2,3-dibromopropanal
folate
Conditions | Yield |
---|---|
With iodine | |
With sodium dichromate |
2,5,6-triamino-3,4-dihydro-4-pyrimidinone
2,3-dibromopropanal
4-amino-benzoic acid
pteroic acid
Conditions | Yield |
---|---|
With ethanol Loesung vom pH 4; |
2,5,6-triamino-3,4-dihydro-4-pyrimidinone
2,3-dibromopropanal
o-toluidine
Conditions | Yield |
---|---|
With sodium dichromate |
p-aminophenylarsonic acid
2,4,5,6-tetraaminopyrimidine
2,3-dibromopropanal
{4-[(2,4-diamino-pteridin-6-ylmethyl)-amino]-phenyl}-arsonic acid
Conditions | Yield |
---|---|
With hydrogenchloride; sodium dichromate; acetic acid pH 3-4; |
2,4,5,6-tetraaminopyrimidine
2,3-dibromopropanal
N-(4-amino-benzoyl)-serine
Conditions | Yield |
---|---|
With water; iodine |
N-(4-aminobenzoyl)-glutamic acid
2-methylsulfanyl-pyrimidine-4,5,6-triamine
2,3-dibromopropanal
N-{4-[(4-amino-2-methylsulfanyl-pteridin-6-ylmethyl)-amino]-benzoyl}-DL-glutamic acid
Conditions | Yield |
---|---|
With sodium acetate |
IUPAC Name: 2,3-Dibromopropanal
Product Name: 2,3-Dibromopropanal
The MF of 2,3-Dibromopropanal (CAS NO.5221-17-0) is C3H4Br2O.
The MW of 2,3-Dibromopropanal (CAS NO.5221-17-0) is 215.8713.
Synonyms of 2,3-Dibromopropanal (CAS NO.5221-17-0): Propanal, 2,3-dibromo- ; 2,3-Dibromopropionaldehyde ; Propanal, 2,3-dibromo- (9CI) ; Propionaldehyde, 2,3-dibromo-
Product Categories: Pharmaceutical Intermediates
Form: Light yellow fuming liquid
EINECS: 226-017-5
Index of Refraction: 1.53
Density: 2.114 g/ml
Flash Point: 88 °C
Boiling Point: 191.9 °C
2,3-Dibromopropanal (CAS NO.5221-17-0) is anti-tumor class medicine for medical methylamine neopterin production,also for other organic synthesis intermediates.
Preparation Products: Folic acid
Raw materials: Carbon tetrachloride-->Acrolein
1. | mmo-sat 1 nmol/plate | MUREAV Mutation Research. 78 (1980),113. | ||
2. | ipr-mus LD50:5 mg/kg | JAFCAU Journal of Agricultural and Food Chemistry. 30 (1982),627. | ||
3. | ivn-mus LD50:56 mg/kg | CSLNX* U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. (Aberdeen Proving Ground, MD 21010) NX#02408 . |
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