Product Name

  • Name

    3,5-DI-T-BUTYL-4-METHOXYBENZALDEHYDE

  • EINECS
  • CAS No. 5221-17-0
  • Article Data24
  • CAS DataBase
  • Density 2.114g/cm3
  • Solubility
  • Melting Point
  • Formula C3H4 Br2 O
  • Boiling Point 191.9°Cat760mmHg
  • Molecular Weight 215.872
  • Flash Point 88°C
  • Transport Information
  • Appearance
  • Safety Poison by intravenous route. Mutagenic data reported. When heated to decomposition it emits toxic fumes of Br. See also ALDEHYDES and BROMIDES.
  • Risk Codes
  • Molecular Structure Molecular Structure of 5221-17-0 (3,5-DI-T-BUTYL-4-METHOXYBENZALDEHYDE)
  • Hazard Symbols
  • Synonyms Propionaldehyde,2,3-dibromo- (7CI,8CI); 2,3-Dibromopropanal; 2,3-Dibromopropional;2,3-Dibromopropionaldehyde; Acrolein dibromide; NSC 6737
  • PSA 17.07000
  • LogP 1.34370

Synthetic route

acrolein
107-02-8

acrolein

2,3-dibromopropanal
5221-17-0

2,3-dibromopropanal

Conditions
ConditionsYield
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
18791-02-1

2,3-dibromo-propionyl chloride

2,3-dibromopropanal
5221-17-0

2,3-dibromopropanal

Conditions
ConditionsYield
With lithium tri(t-butoxy)aluminum hydride In tetrahydrofuran Reduction;79%
3,4-dibromo-1-butene
10463-48-6

3,4-dibromo-1-butene

A

formaldehyd
50-00-0

formaldehyd

B

2,3-dibromopropanal
5221-17-0

2,3-dibromopropanal

Conditions
ConditionsYield
bei der Ozonspaltung;
1,3-dibromo-propane
109-64-8

1,3-dibromo-propane

2,3-dibromopropanal
5221-17-0

2,3-dibromopropanal

Conditions
ConditionsYield
With water; bromine
acrolein
107-02-8

acrolein

A

2,3-dibromopropanal
5221-17-0

2,3-dibromopropanal

B

2,3,3-tribromo-propionaldehyde

2,3,3-tribromo-propionaldehyde

Conditions
ConditionsYield
With bromine
1,3-dibromopropene
627-15-6

1,3-dibromopropene

aqueous bromine

aqueous bromine

2,3-dibromopropanal
5221-17-0

2,3-dibromopropanal

4,5-dibromo-pent-2-enoic acid
85858-56-6

4,5-dibromo-pent-2-enoic acid

chloroform
67-66-3

chloroform

water
7732-18-5

water

A

2,3-dibromopropanal
5221-17-0

2,3-dibromopropanal

B

oxasoic acid

oxasoic acid

2,3-dibromopropanal
5221-17-0

2,3-dibromopropanal

N-(1-trifluoromethyltrifluoroethylidene)-2-trifluoromethyl-3,3,3-trifluoropropionamide
35933-97-2

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
83926-93-6

2-(1,2-dibromoethyl)-4,4-bis(trifluoromethyl)-6-(2-hydrohexafluoroisopropyl)-2H,4H-1,3,5-dioxazine

Conditions
ConditionsYield
In tetrachloromethane at 100℃; for 1h;94.8%
2,3-dibromopropanal
5221-17-0

2,3-dibromopropanal

meso-2,3-Dimercaptobernsteinsaeure-dimethylester
17660-57-0

meso-2,3-Dimercaptobernsteinsaeure-dimethylester

(4R,5S)-2-(1,2-Dibromo-ethyl)-[1,3]dithiolane-4,5-dicarboxylic acid dimethyl ester

(4R,5S)-2-(1,2-Dibromo-ethyl)-[1,3]dithiolane-4,5-dicarboxylic acid dimethyl ester

Conditions
ConditionsYield
With toluene-4-sulfonic acid90%
2,3-dibromopropanal
5221-17-0

2,3-dibromopropanal

sodium benzenesulfonate
873-55-2

sodium benzenesulfonate

(E)-3-(phenylsulfonyl)acrylaldehyde

(E)-3-(phenylsulfonyl)acrylaldehyde

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 20℃; for 20h;76%
2,3-dibromopropanal
5221-17-0

2,3-dibromopropanal

trimethyleneglycol
504-63-2

trimethyleneglycol

2-(1,2-dibromoethyl)-1,3-dioxane
89791-57-1

2-(1,2-dibromoethyl)-1,3-dioxane

Conditions
ConditionsYield
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
5221-17-0

2,3-dibromopropanal

ethylene glycol
107-21-1

ethylene glycol

2-(1',2'-dibromoethyl)-1,3-dioxolane
5267-72-1

2-(1',2'-dibromoethyl)-1,3-dioxolane

Conditions
ConditionsYield
With cationite KU-2-8 In benzene Heating;71%
2,3-dibromopropanal
5221-17-0

2,3-dibromopropanal

2,2-Dimethyl-1,3-propanediol
126-30-7

2,2-Dimethyl-1,3-propanediol

2-(1,2-dibromoethyl)-5,5-dimethyl-1,3-dioxane

2-(1,2-dibromoethyl)-5,5-dimethyl-1,3-dioxane

Conditions
ConditionsYield
With cationite KU-2-8 In benzene Heating;64%
diethyl ether
60-29-7

diethyl ether

2,3-dibromopropanal
5221-17-0

2,3-dibromopropanal

3,4-dibromobutan-2-one
25109-57-3

3,4-dibromobutan-2-one

2,3-dibromopropanal
5221-17-0

2,3-dibromopropanal

3,4-dibromobutan-2-one
25109-57-3

3,4-dibromobutan-2-one

Conditions
ConditionsYield
With diethyl ether
1,4-dioxane
123-91-1

1,4-dioxane

2,3-dibromopropanal
5221-17-0

2,3-dibromopropanal

N-methyl-p-aminobenzoic acid
10541-83-0

N-methyl-p-aminobenzoic acid

6-carboxy-1-methyl-quinolinium; bromide

6-carboxy-1-methyl-quinolinium; bromide

1,4-dioxane
123-91-1

1,4-dioxane

2,3-dibromopropanal
5221-17-0

2,3-dibromopropanal

4-(benzyl-methyl-amino)-benzoic acid
25070-91-1

4-(benzyl-methyl-amino)-benzoic acid

6-carboxy-1-methyl-quinolinium; bromide

6-carboxy-1-methyl-quinolinium; bromide

pyridine
110-86-1

pyridine

2,3-dibromopropanal
5221-17-0

2,3-dibromopropanal

1-(2-amino-4-oxo-3,4-dihydro-pteridin-6-ylmethyl)-pyridinium; iodide

1-(2-amino-4-oxo-3,4-dihydro-pteridin-6-ylmethyl)-pyridinium; iodide

Conditions
ConditionsYield
und Behandeln des erhaltenen Reaktionsprodukts mit 2,5,6-Triamino-3H-pyrimidin-4-on und KI;
methanol
67-56-1

methanol

2,3-dibromopropanal
5221-17-0

2,3-dibromopropanal

formimidomethylester hydrochloride
15755-09-6

formimidomethylester hydrochloride

1,2-dibromo-3,3-dimethoxypropane
248955-54-6

1,2-dibromo-3,3-dimethoxypropane

4,5,6-triamino-1H-pyrimidine-2-thione
1073-99-0

4,5,6-triamino-1H-pyrimidine-2-thione

2,3-dibromopropanal
5221-17-0

2,3-dibromopropanal

N-(4-aminobenzoyl)-L-glutamic acid
4271-30-1

N-(4-aminobenzoyl)-L-glutamic acid

N-{4-[(4-amino-2-thioxo-1,2-dihydro-pteridin-6-ylmethyl)-amino]-benzoyl}-L-glutamic acid
103207-69-8

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
1073-99-0

4,5,6-triamino-1H-pyrimidine-2-thione

2,3-dibromopropanal
5221-17-0

2,3-dibromopropanal

4-amino-benzoic acid
150-13-0

4-amino-benzoic acid

4-[(4-amino-2-thioxo-1,2-dihydro-pteridin-6-ylmethyl)-amino]-benzoic acid
92253-82-2

4-[(4-amino-2-thioxo-1,2-dihydro-pteridin-6-ylmethyl)-amino]-benzoic acid

5,6-diaminouracil
3240-72-0

5,6-diaminouracil

2,3-dibromopropanal
5221-17-0

2,3-dibromopropanal

N-(4-aminobenzoyl)-L-glutamic acid
4271-30-1

N-(4-aminobenzoyl)-L-glutamic acid

N-{4-[(2,4-dioxo-1,2,3,4-tetrahydro-pteridin-6-ylmethyl)-amino]-benzoyl}-L-glutamic acid
25663-25-6

N-{4-[(2,4-dioxo-1,2,3,4-tetrahydro-pteridin-6-ylmethyl)-amino]-benzoyl}-L-glutamic acid

Conditions
ConditionsYield
With sodium acetate; acetic acid
N-(4-aminobenzoyl)-B-alanine
7377-08-4

N-(4-aminobenzoyl)-B-alanine

2,5,6-triamino-3,4-dihydro-4-pyrimidinone
1004-75-7

2,5,6-triamino-3,4-dihydro-4-pyrimidinone

2,3-dibromopropanal
5221-17-0

2,3-dibromopropanal

N-pteroyl-β-alanine
15677-93-7

N-pteroyl-β-alanine

Conditions
ConditionsYield
With sodium dichromate
With iodine
2,5,6-triamino-3,4-dihydro-4-pyrimidinone
1004-75-7

2,5,6-triamino-3,4-dihydro-4-pyrimidinone

2,3-dibromopropanal
5221-17-0

2,3-dibromopropanal

N-methyl-p-aminobenzoic acid
10541-83-0

N-methyl-p-aminobenzoic acid

10-methyl-pteroic acid
5623-18-7

10-methyl-pteroic acid

2,5,6-triamino-3,4-dihydro-4-pyrimidinone
1004-75-7

2,5,6-triamino-3,4-dihydro-4-pyrimidinone

2,3-dibromopropanal
5221-17-0

2,3-dibromopropanal

4-(N-butylamino)benzoic acid
4740-24-3

4-(N-butylamino)benzoic acid

10-butyl-pteroic acid

10-butyl-pteroic acid

2,5,6-triamino-3,4-dihydro-4-pyrimidinone
1004-75-7

2,5,6-triamino-3,4-dihydro-4-pyrimidinone

2,3-dibromopropanal
5221-17-0

2,3-dibromopropanal

N-(4-amino-benzoyl)-alanine
99146-89-1

N-(4-amino-benzoyl)-alanine

N-pteroyl-DL-alanine

N-pteroyl-DL-alanine

Conditions
ConditionsYield
With sodium dichromate
With iodine
2,5,6-triamino-3,4-dihydro-4-pyrimidinone
1004-75-7

2,5,6-triamino-3,4-dihydro-4-pyrimidinone

2,3-dibromopropanal
5221-17-0

2,3-dibromopropanal

p-(N-methylamino)benzoyl-L-glutamic acid
52980-68-4

p-(N-methylamino)benzoyl-L-glutamic acid

N10-methylfolic acid
2410-93-7

N10-methylfolic acid

2,5,6-triamino-3,4-dihydro-4-pyrimidinone
1004-75-7

2,5,6-triamino-3,4-dihydro-4-pyrimidinone

2,3-dibromopropanal
5221-17-0

2,3-dibromopropanal

N-(4-amino-3-methyl-benzoyl)-L-glutamic acid
875430-61-8

N-(4-amino-3-methyl-benzoyl)-L-glutamic acid

N-(3'-methyl-pteroyl)-L-glutamic acid

N-(3'-methyl-pteroyl)-L-glutamic acid

N-(4-aminobenzoyl)-glutamic acid
4230-33-5

N-(4-aminobenzoyl)-glutamic acid

2,5,6-triamino-3,4-dihydro-4-pyrimidinone
1004-75-7

2,5,6-triamino-3,4-dihydro-4-pyrimidinone

2,3-dibromopropanal
5221-17-0

2,3-dibromopropanal

folate
65165-92-6

folate

2,5,6-triamino-3,4-dihydro-4-pyrimidinone
1004-75-7

2,5,6-triamino-3,4-dihydro-4-pyrimidinone

2,3-dibromopropanal
5221-17-0

2,3-dibromopropanal

(4-amino-benzoylamino)-malonic acid

(4-amino-benzoylamino)-malonic acid

pteroylamino-malonic acid

pteroylamino-malonic acid

Conditions
ConditionsYield
With iodine
With sodium dichromate
2,5,6-triamino-3,4-dihydro-4-pyrimidinone
1004-75-7

2,5,6-triamino-3,4-dihydro-4-pyrimidinone

2,3-dibromopropanal
5221-17-0

2,3-dibromopropanal

4-amino-benzoic acid
150-13-0

4-amino-benzoic acid

pteroic acid
119-24-4

pteroic acid

Conditions
ConditionsYield
With ethanol Loesung vom pH 4;
2,5,6-triamino-3,4-dihydro-4-pyrimidinone
1004-75-7

2,5,6-triamino-3,4-dihydro-4-pyrimidinone

2,3-dibromopropanal
5221-17-0

2,3-dibromopropanal

o-toluidine
95-53-4

o-toluidine

2-amino-6-o-toluidinomethyl-3H-pteridin-4-one

2-amino-6-o-toluidinomethyl-3H-pteridin-4-one

Conditions
ConditionsYield
With sodium dichromate
p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

2,4,5,6-tetraaminopyrimidine
1004-74-6

2,4,5,6-tetraaminopyrimidine

2,3-dibromopropanal
5221-17-0

2,3-dibromopropanal

{4-[(2,4-diamino-pteridin-6-ylmethyl)-amino]-phenyl}-arsonic acid
109160-53-4

{4-[(2,4-diamino-pteridin-6-ylmethyl)-amino]-phenyl}-arsonic acid

Conditions
ConditionsYield
With hydrogenchloride; sodium dichromate; acetic acid pH 3-4;
2,4,5,6-tetraaminopyrimidine
1004-74-6

2,4,5,6-tetraaminopyrimidine

2,3-dibromopropanal
5221-17-0

2,3-dibromopropanal

N-(4-amino-benzoyl)-serine
879278-42-9

N-(4-amino-benzoyl)-serine

N-{4-[(2,4-diamino-pteridin-6-ylmethyl)-amino]-benzoyl}-DL-serine

N-{4-[(2,4-diamino-pteridin-6-ylmethyl)-amino]-benzoyl}-DL-serine

Conditions
ConditionsYield
With water; iodine
N-(4-aminobenzoyl)-glutamic acid
4230-33-5

N-(4-aminobenzoyl)-glutamic acid

2-methylsulfanyl-pyrimidine-4,5,6-triamine
1431-40-9

2-methylsulfanyl-pyrimidine-4,5,6-triamine

2,3-dibromopropanal
5221-17-0

2,3-dibromopropanal

N-{4-[(4-amino-2-methylsulfanyl-pteridin-6-ylmethyl)-amino]-benzoyl}-DL-glutamic acid
94543-82-5

N-{4-[(4-amino-2-methylsulfanyl-pteridin-6-ylmethyl)-amino]-benzoyl}-DL-glutamic acid

Conditions
ConditionsYield
With sodium acetate

2,3-Dibromopropanal Chemical Properties

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 Uses

  2,3-Dibromopropanal (CAS NO.5221-17-0) is anti-tumor class medicine for medical methylamine neopterin production,also for other organic synthesis intermediates.

2,3-Dibromopropanal Production

Preparation Products: Folic acid
Raw materials: Carbon tetrachloride-->Acrolein

2,3-Dibromopropanal Toxicity Data With Reference

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 .

2,3-Dibromopropanal Safety Profile

Poison by intravenous route. Mutagenic data reported. When heated to decomposition it emits toxic fumes of Br. See also ALDEHYDES and BROMIDES.

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