Product Name

  • Name

    2-Methylpropanedioic acid

  • EINECS 208-219-5
  • CAS No. 516-05-2
  • Article Data55
  • CAS DataBase
  • Density 1.402 g/cm3
  • Solubility Soluble in water
  • Melting Point 128-130 °C(lit.)
  • Formula C4H6O4
  • Boiling Point 334.4 °C at 760 mmHg
  • Molecular Weight 118.089
  • Flash Point 170.2 °C
  • Transport Information
  • Appearance white crystals
  • Safety 26
  • Risk Codes 36/37/38
  • Molecular Structure Molecular Structure of 516-05-2 (2-Methylpropanedioic acid)
  • Hazard Symbols IrritantXi
  • Synonyms CPD-546;Propanedioic acid, methyl-;2-methylpropanedioic acid;2-methylpropanedioate;Propanedioic acid, methyl- (9CI);2-Methylmalonic acid;methylpropanedioic acid;4-02-00-01932 (Beilstein Handbook Reference);Malonic acid, methyl-;1, 1-Ethanedicarboxylic acid;Isosuccinic acid;
  • PSA 74.60000
  • LogP -0.20830

Synthetic route

Diethyl methylmalonate
609-08-5

Diethyl methylmalonate

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

Conditions
ConditionsYield
With potassium hydroxide In ethanol for 1h; Ambient temperature;99%
With potassium hydroxide In water at 0 - 20℃; for 60h;71%
With potassium hydroxide In ethanol; water for 4h; Heating;
monomethyl monopotassium malonate
38330-80-2

monomethyl monopotassium malonate

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

Conditions
ConditionsYield
With concentrated hydrochloric acid In water96%
With hydrogenchloride In hexane; dichloromethane84.8%
1,3-di-tert-butyl 2-methylpropanedioate
34812-95-8

1,3-di-tert-butyl 2-methylpropanedioate

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

Conditions
ConditionsYield
With sodium hydroxide In methanol; dichloromethane at 20℃; for 3h; Solvent;84%
methyl-malonic acid dimethylester
609-02-9

methyl-malonic acid dimethylester

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

Conditions
ConditionsYield
In water; toluene81%
With sodium hydroxide In methanol at 20℃;
With water; sodium hydroxide In methanol at 80℃; for 1h;
2-cyanopropanoic acid
632-07-5

2-cyanopropanoic acid

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

Conditions
ConditionsYield
With potassium hydroxide
2-methylmalonyl dichloride
39619-07-3

2-methylmalonyl dichloride

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

Conditions
ConditionsYield
With sodium hydroxide
2-methyl-1.3-propanediol
2163-42-0

2-methyl-1.3-propanediol

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

Conditions
ConditionsYield
With nitric acid
(2RS)-3,3,3-trifluoro-2-methylpropanoic acid
381-97-5

(2RS)-3,3,3-trifluoro-2-methylpropanoic acid

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

Conditions
ConditionsYield
With sodium hydroxide
2-cyano-3-imino-4-methyl-glutaric acid-1-ethyl ester

2-cyano-3-imino-4-methyl-glutaric acid-1-ethyl ester

furan-2,3,5(4H)-trione pyridine (1:1)

furan-2,3,5(4H)-trione pyridine (1:1)

A

malonic acid
141-82-2

malonic acid

B

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

Conditions
ConditionsYield
Kochen;
2-cyano-3-imino-4-methyl-glutaric acid diethyl ester

2-cyano-3-imino-4-methyl-glutaric acid diethyl ester

furan-2,3,5(4H)-trione pyridine (1:1)

furan-2,3,5(4H)-trione pyridine (1:1)

A

malonic acid
141-82-2

malonic acid

B

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

2-cyano-3-imino-2,4,4-trimethyl-glutaric acid diethyl ester

2-cyano-3-imino-2,4,4-trimethyl-glutaric acid diethyl ester

furan-2,3,5(4H)-trione pyridine (1:1)

furan-2,3,5(4H)-trione pyridine (1:1)

A

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

B

2,2-dimethylmalonic acid
595-46-0

2,2-dimethylmalonic acid

Conditions
ConditionsYield
Erhitzen;
methyl-malonyl bromide
98020-11-2

methyl-malonyl bromide

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

Conditions
ConditionsYield
With water
propionyl chloride
79-03-8

propionyl chloride

trichloromethyl chloroformate
503-38-8

trichloromethyl chloroformate

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

Conditions
ConditionsYield
at 225℃; folgendes Verseifen mit Wasser;
at 225℃; im Rohr; und folgende Hydrolyse;
at 225℃; folgendes Verseifen mit Wasser;
potassium cyanide
151-50-8

potassium cyanide

Ethyl 2-bromopropionate
535-11-5, 41978-69-2

Ethyl 2-bromopropionate

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

Conditions
ConditionsYield
With ethanol ueber mehreren Stufen;
2-methyl-3-oxo-3-(phenylamino)propanoic acid
15601-92-0

2-methyl-3-oxo-3-(phenylamino)propanoic acid

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

Conditions
ConditionsYield
With sodium hydroxide Heating;
ethene
74-85-1

ethene

carbon dioxide
124-38-9

carbon dioxide

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

Conditions
ConditionsYield
1.) Al, AlCl3, methylcyclohexane, 3 atm, 90-95 deg C, 12h; 2.) methylcyclohexane, 75 atm, 80 deg C; Multistep reaction;
malonic acid
141-82-2

malonic acid

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

Conditions
ConditionsYield
With sodium bromate; sulfuric acid; cerium (IV) sulfate In water at 25℃; Mechanism;
ethyl 2-nitrophenyl methylmalonate
24161-56-6

ethyl 2-nitrophenyl methylmalonate

A

ethanol
64-17-5

ethanol

B

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

C

2-hydroxynitrobenzene
88-75-5

2-hydroxynitrobenzene

Conditions
ConditionsYield
With pH = 8.00 In water at 23℃; under 750.06 Torr; Mechanism; Rate constant; pressure-dependence of rates of elimination; activation parameter for hydrolysis: ΔV(excit.); var. press.;
3,3-Dihydroxy-2-methyl-acrylic acid
69858-40-8

3,3-Dihydroxy-2-methyl-acrylic acid

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

Conditions
ConditionsYield
With cis-nitrous acid; chloride In water at 25℃; Equilibrium constant;
chloroethane
75-00-3

chloroethane

carbon dioxide
124-38-9

carbon dioxide

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

Conditions
ConditionsYield
With sodium; Petroleum ether at 110℃; unter Druck;
2-methyl-1.3-propanediol
2163-42-0

2-methyl-1.3-propanediol

nitric acid
7697-37-2

nitric acid

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

carbon dioxide
124-38-9

carbon dioxide

diethylmercury
627-44-1

diethylmercury

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

Conditions
ConditionsYield
With sodium; Petroleum ether at 110℃; unter Druck;
(2RS)-3,3,3-trifluoro-2-methylpropanoic acid
381-97-5

(2RS)-3,3,3-trifluoro-2-methylpropanoic acid

aqueous NaOH-solution

aqueous NaOH-solution

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

isosuccinic acid amide

isosuccinic acid amide

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

Conditions
ConditionsYield
With sodium hydroxide
2-methyl-1.3-propanediol
2163-42-0

2-methyl-1.3-propanediol

KMnO4

KMnO4

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

2-cyano-3-imino-2,4-dimethyl-glutaric acid diethyl ester

2-cyano-3-imino-2,4-dimethyl-glutaric acid diethyl ester

strong KOH-solution

strong KOH-solution

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

Conditions
ConditionsYield
Erhitzen;
ethyl 3-bromo-2-(ethoxycarbonyl)propionate
34762-17-9

ethyl 3-bromo-2-(ethoxycarbonyl)propionate

acetic acid
64-19-7

acetic acid

zinc

zinc

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

4-cyano-2-methyl-3-oxo-valeric acid ethyl ester
872822-99-6

4-cyano-2-methyl-3-oxo-valeric acid ethyl ester

alkali, aqueous

alkali, aqueous

A

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

B

propionic acid
802294-64-0

propionic acid

Conditions
ConditionsYield
Hydrolysis;
chloroethane
75-00-3

chloroethane

carbon dioxide
124-38-9

carbon dioxide

sodium

sodium

ligroine

ligroine

A

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

B

propionic acid
802294-64-0

propionic acid

Conditions
ConditionsYield
at 110℃; under 11032.6 Torr;
9-hydroxyxanthene
90-46-0

9-hydroxyxanthene

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

(±)-2-(9H-xanthen-9-yl)propanoic acid
150330-35-1

(±)-2-(9H-xanthen-9-yl)propanoic acid

Conditions
ConditionsYield
With pyrrolidine; isopropyl alcohol; potassium hydroxide In toluene for 24h; Reflux;99%
With pyridine
5-(4'-fluorophenyl)furan-2-carbaldehyde
33342-17-5

5-(4'-fluorophenyl)furan-2-carbaldehyde

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

(E)-2-methyl-3-(5-(4-fluorophenyl)furan-2-yl)acrylic acid

(E)-2-methyl-3-(5-(4-fluorophenyl)furan-2-yl)acrylic acid

Conditions
ConditionsYield
With piperidine; pyridine for 3h; Knoevenagel Condensation; Reflux;96.7%
methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

disilver methylmalonate

disilver methylmalonate

Conditions
ConditionsYield
With sodium hydroxide; nitric acid; silver nitrate In methanol; water96.7%
methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

4-(4-methylphenyl)thiophene-2-carbaldehyde
853311-16-7

4-(4-methylphenyl)thiophene-2-carbaldehyde

(E)-2-methyl-3-(4-(4-methylphenyl)thiophen-2-yl)acrylic acid

(E)-2-methyl-3-(4-(4-methylphenyl)thiophen-2-yl)acrylic acid

Conditions
ConditionsYield
With piperidine; pyridine for 3h; Knoevenagel Condensation; Reflux;96.1%
piperidine
110-89-4

piperidine

tert-butyl (+/-)-trans-2,2-dimethyl-3-formylcyclopropanecarboxylate

tert-butyl (+/-)-trans-2,2-dimethyl-3-formylcyclopropanecarboxylate

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

tert-butyl (+/-)-trans-2,2-dimethyl-3-{2-carboxy-(E)-1-propenyl}cyclopropanecarboxylate
1195315-35-5

tert-butyl (+/-)-trans-2,2-dimethyl-3-{2-carboxy-(E)-1-propenyl}cyclopropanecarboxylate

Conditions
ConditionsYield
In pyridine; diethyl ether; hexane; ethyl acetate96%
In pyridine; diethyl ether; hexane; ethyl acetate94.1%
4-phenylthiophene-2-carbaldehyde
26170-87-6

4-phenylthiophene-2-carbaldehyde

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

(E)-2-methyl-3-(4-phenylthiophen-2-yl)acrylic acid
941281-24-9

(E)-2-methyl-3-(4-phenylthiophen-2-yl)acrylic acid

Conditions
ConditionsYield
With piperidine; pyridine for 3h; Knoevenagel Condensation; Reflux;95.5%
methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

3-methyl-2-methylthio-6-(tetra-O-acetyl-β-D-glucopyranosylamino)pyrimidin-4(3H)-one
94940-17-7

3-methyl-2-methylthio-6-(tetra-O-acetyl-β-D-glucopyranosylamino)pyrimidin-4(3H)-one

3,4,7,8-tetrahydro-5-hydroxy-3,6-dimethyl-2-methylthio-4,7-dioxo-8-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)pyrido<2,3-d>pyrimidine
135112-04-8

3,4,7,8-tetrahydro-5-hydroxy-3,6-dimethyl-2-methylthio-4,7-dioxo-8-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)pyrido<2,3-d>pyrimidine

Conditions
ConditionsYield
With acetic anhydride at 100℃; for 1h;95%
methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

di-tert-butyl dicarbonate
24424-99-5

di-tert-butyl dicarbonate

1,3-di-tert-butyl 2-methylpropanedioate
34812-95-8

1,3-di-tert-butyl 2-methylpropanedioate

Conditions
ConditionsYield
With dmap In diethyl ether; tert-butyl alcohol at 23℃; for 48h; Inert atmosphere;95%
methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

calcium 2-methylmalonate

calcium 2-methylmalonate

Conditions
ConditionsYield
With calcium hydroxide In water at 70℃; for 5h;95%
methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

allyl alcohol
107-18-6

allyl alcohol

2-methylmalonic acid diallyl ester
150193-37-6

2-methylmalonic acid diallyl ester

Conditions
ConditionsYield
With toluene-4-sulfonic acid In benzene Heating;92%
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 0 - 20℃; for 3.08333h;
methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

5-(4-tolyl)-2-furaldehyde
34035-05-7

5-(4-tolyl)-2-furaldehyde

(E)-2-methyl-3-(5-(4-methylphenyl)furan-2-yl)acrylic acid

(E)-2-methyl-3-(5-(4-methylphenyl)furan-2-yl)acrylic acid

Conditions
ConditionsYield
With piperidine; pyridine for 3h; Knoevenagel Condensation; Reflux;92%
methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

4-(4-fluorophenyl)furan-2-carbaldehyde

4-(4-fluorophenyl)furan-2-carbaldehyde

(E)-2-methyl-3-(4-(4-fluorophenyl)furan-2-yl)acrylic acid

(E)-2-methyl-3-(4-(4-fluorophenyl)furan-2-yl)acrylic acid

Conditions
ConditionsYield
With piperidine; pyridine for 3h; Knoevenagel Condensation; Reflux;91.3%
1,2-dimethoxybenzene
91-16-7

1,2-dimethoxybenzene

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

5,6-dimethoxy-2-methyl-1H-indene-1,3(2H)-dione
738616-34-7

5,6-dimethoxy-2-methyl-1H-indene-1,3(2H)-dione

Conditions
ConditionsYield
In dichloromethane at 22℃; for 18h;91%
With Eaton’s reagent In dichloromethane at 22℃; for 18h; Inert atmosphere;66%
1-(2-fluoro-4-iodophenyl)-3-(4-methoxybenzyl)-6-(methylamino)pyrimidine-2,4(1H,3H)-dione
871700-54-8

1-(2-fluoro-4-iodophenyl)-3-(4-methoxybenzyl)-6-(methylamino)pyrimidine-2,4(1H,3H)-dione

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

1-(2-fluoro-4-iodophenyl)-5-hydroxy-3-(4-methoxybenzyl)-6,8-dimethylpyrido[2,3-d]pyrimidine-2,4,7(1H,3H,8H)-trione
871700-55-9

1-(2-fluoro-4-iodophenyl)-5-hydroxy-3-(4-methoxybenzyl)-6,8-dimethylpyrido[2,3-d]pyrimidine-2,4,7(1H,3H,8H)-trione

Conditions
ConditionsYield
With acetic anhydride at 90 - 100℃; for 4h;90.7%
methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

4-(3,4-methylene-dioxyphenyl)thiophene-2-carbaldehyde

4-(3,4-methylene-dioxyphenyl)thiophene-2-carbaldehyde

(E)-2-methyl-3-(4-(3,4-methylene-dioxyphenyl)thiophen-2-yl)acrylic acid

(E)-2-methyl-3-(4-(3,4-methylene-dioxyphenyl)thiophen-2-yl)acrylic acid

Conditions
ConditionsYield
With piperidine; pyridine for 3h; Knoevenagel Condensation; Reflux;90.6%
methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

butan-1-ol
71-36-3

butan-1-ol

dibutyl 2-methylmalonate
52886-83-6

dibutyl 2-methylmalonate

Conditions
ConditionsYield
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 0 - 20℃; for 3.08333h;90%
methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

isopropyl alcohol
67-63-0

isopropyl alcohol

diisopropyl 2-methylmalonate

diisopropyl 2-methylmalonate

Conditions
ConditionsYield
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 0 - 20℃; for 3.08333h;90%
methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

cyclohexanol
108-93-0

cyclohexanol

dicyclohexyl 2-methylmalonate
73742-26-4

dicyclohexyl 2-methylmalonate

Conditions
ConditionsYield
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 0 - 20℃; for 3.08333h;90%
2-methoxy-ethanol
109-86-4

2-methoxy-ethanol

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

bis(2-methoxyethyl) 2-methylmalonate

bis(2-methoxyethyl) 2-methylmalonate

Conditions
ConditionsYield
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 0 - 20℃; for 3.08333h;90%
methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

4-(4-nitrophenyl)thiophene-2-carbaldehyde

4-(4-nitrophenyl)thiophene-2-carbaldehyde

(E)-2-methyl-3-(4-(4-nitrophenyl)thiophen-2-yl)acrylic acid

(E)-2-methyl-3-(4-(4-nitrophenyl)thiophen-2-yl)acrylic acid

Conditions
ConditionsYield
With piperidine; pyridine for 3h; Knoevenagel Condensation; Reflux;89.4%
methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

2,4,6-Trichlorophenol
88-06-2

2,4,6-Trichlorophenol

bis(2,4,6-trichlorophenyl) 2-methylmalonate
15781-71-2

bis(2,4,6-trichlorophenyl) 2-methylmalonate

Conditions
ConditionsYield
With trichlorophosphate for 5h; Reflux;89.11%
With trichlorophosphate Reflux;
N,N'-dimesitylformamidine
75105-48-5

N,N'-dimesitylformamidine

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

1,3-dimesityl-5-methyl-6-oxo-6H-pyrimidinium-4-olate
1051375-11-1

1,3-dimesityl-5-methyl-6-oxo-6H-pyrimidinium-4-olate

Conditions
ConditionsYield
With dicyclohexyl-carbodiimide In dichloromethane at 20℃; for 3h; Inert atmosphere;89%
With triethylamine; dicyclohexyl-carbodiimide In dichloromethane at 0℃; Schlenk technique; Inert atmosphere;89%
4,4'-bipyridine
553-26-4

4,4'-bipyridine

zinc(II) nitrate hexahydrate

zinc(II) nitrate hexahydrate

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

[Zn2(4,4′-bpy)(Memal)2(H2O)2]n

[Zn2(4,4′-bpy)(Memal)2(H2O)2]n

Conditions
ConditionsYield
With sodium carbonate In methanol; water three parts sepd. by water interphases: aq. soln. of MeCH(CO2H)2 and Na2CO3 at the bottom, soln. of Zn nitrate in the middle region and soln. ofbipyridine in MeOH on the top; sysztem stored at room temp. for a few w k; crystals collected; washed with H2O/EtOH; air dried; elem. anal.;89%
methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

1,1-di(p-tolyl)ethylene
2919-20-2

1,1-di(p-tolyl)ethylene

2-carboxy-2-methyl-4,4-bis(4-methylphenyl)-4-butanolide

2-carboxy-2-methyl-4,4-bis(4-methylphenyl)-4-butanolide

Conditions
ConditionsYield
With manganese triacetate In acetic acid at 100℃; for 0.05h;88%
methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

4-(6-fluoropyridin-3-yl)furan-2-carbaldehyde

4-(6-fluoropyridin-3-yl)furan-2-carbaldehyde

(E)-2-methyl-3-(4-(6-fluoropyridin-3-yl)furan-2-yl)acrylic acid

(E)-2-methyl-3-(4-(6-fluoropyridin-3-yl)furan-2-yl)acrylic acid

Conditions
ConditionsYield
With piperidine; pyridine for 3h; Knoevenagel Condensation; Reflux;87.7%
methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

1,1'-(4-nitro-phenylmethanediyl)-bis-piperidine
55591-35-0

1,1'-(4-nitro-phenylmethanediyl)-bis-piperidine

(E)-2-methyl-3-(4-nitrophenyl)acrylic acid
13048-77-6, 949-98-4, 13048-76-5

(E)-2-methyl-3-(4-nitrophenyl)acrylic acid

Conditions
ConditionsYield
for 96h; Ambient temperature;87%
4,4'-bipyridine
553-26-4

4,4'-bipyridine

cobalt(II) nitrate hexahydrate

cobalt(II) nitrate hexahydrate

methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

[Co(II)2(4,4'-bipyridine)(methylmalonate(2-))2(H2O)2]

[Co(II)2(4,4'-bipyridine)(methylmalonate(2-))2(H2O)2]

Conditions
ConditionsYield
With sodium carbonate In methanol; water three parts sepd. by water interphases: aq. soln. of MeCH(CO2H)2 and Na2CO3 at the bottom, soln. of CoCl2*6H2O in the middle region and soln. ofbipyridine in MeOH on the top; system stored at room temp. for a few wk; crystals collected; washed with H2O/EtOH; air dried; elem. anal.;87%
methyl-propanedioic acid
516-05-2

methyl-propanedioic acid

Acetic acid (2R,3R,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-(2-methoxy-6-oxo-1,6-dihydro-pyrimidin-4-ylamino)-tetrahydro-pyran-3-yl ester
94940-33-7

Acetic acid (2R,3R,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-(2-methoxy-6-oxo-1,6-dihydro-pyrimidin-4-ylamino)-tetrahydro-pyran-3-yl ester

4-Acetoxy-3-methyl-7-methoxy-5-(2,3,4,6-tetra-O-acetyl-β-D-glucyopyranosylamino)pyrano<2,3-d>pyrimidin-2-one

4-Acetoxy-3-methyl-7-methoxy-5-(2,3,4,6-tetra-O-acetyl-β-D-glucyopyranosylamino)pyrano<2,3-d>pyrimidin-2-one

Conditions
ConditionsYield
With acetic anhydride at 100℃; for 1h;86%

Methylmalonic acid Chemical Properties

The molecular formula of Methylmalonic acid(516-05-2) is C4H6O4 and its formula weight is 118.09.
The density of Methylmalonic acid(516-05-2)  is 1.45  and it has a melting point of 128-130 °C(lit.).
The chemical synonyms of Methylmalonic acid(516-05-2) are METHYLMALONIC ACID;METHYLPROPANEDIOIC ACID;2-METHYLPROPANEDIOIC ACID;PROPANEDIOIC ACID, METHYL-;1,1-Ethanedicarboxylic acid;1,1-ethanedicarboxylicacid;2-Methylmalonic acid;2-methylmalonicacid
The molecular structure of Methylmalonic acid(516-05-2):

Methylmalonic acid Toxicity Data With Reference

RTECS#: CAS# 516-05-2: OO1400000 
LD50/LC50: RTECS: Not available. 
Carcinogenicity: Methylmalonic acid - Not listed as a carcinogen by ACGIH, IARC, NTP, or CA Prop 65.
Other: See actual entry in RTECS for complete information.

Methylmalonic acid Safety Profile

Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26
WGK Germany  3
RTECS  OO1400000

Methylmalonic acid Specification

Chemical Stability: Stable under normal temperatures and pressures. 
Conditions to Avoid: Strong oxidants. 
Incompatibilities with Other Materials Not available 
Hazardous Decomposition Products Irritating and toxic fumes and gases. 
Hazardous Polymerization Hazardous Polymerization 
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