Propanoicacid, 2-hydroxy-, ethyl ester, (2R)- supplier

Name
(+)-ETHYL D-LACTATE
EINECS
CAS No. 7699-00-5
Article Data57
CAS DataBase
Density 1.05 g/cm³
Solubility
Melting Point
Formula C₅H₁₀O₃
Boiling Point 154.5 °C at 760 mmHg
Molecular Weight 118.133
Flash Point 54.6 °C
Transport Information UN 1192 3/PG 3
Appearance
Safety 24-26-39
Risk Codes 10-37-41
Molecular Structure
Hazard Symbols Xi
Synonyms Lacticacid, ethyl ester, D- (8CI);Propanoic acid, 2-hydroxy-, ethyl ester, (R)-;(+)-Ethyl 2-hydroxypropanoate;(+)-Ethyl 2-hydroxypropionate;(+)-Ethyllactate;(2R)-2-Hydroxypropanoic acid ethyl ester;(R)-(+)-Ethyl lactate;(R)-(+)-Lactic acid ethyl ester;(R)-2-Hydroxypropionic acid ethyl ester;(R)-Ethyl lactate;(R)-Lactic acid ethyl ester;D-Ethyl lactate;Ethyl(R)-2-hydroxypropanoate;Ethyl (R)-2-hydroxypropionate;Ethyl D-lactate;
PSA 46.53000
LogP -0.06970

Synthetic route

: 64-17-5
ethanol

: 10326-41-7
D-Lactic acid

: 7699-00-5
(R)-Ethyl lactate

Conditions

Conditions	Yield
With salicylaldehyde at 80℃; for 28h; Inert atmosphere; chemoselective reaction;	85%
With sulfuric acid at 120℃; for 8h; Molecular sieve;	25%
With hydrogenchloride
With sulfuric acid; benzene durch azeotrope Destillation;

: 64-17-5
ethanol

: 104196-77-2, 104264-83-7
(3R,5S,6R,9S)-3,9-Dimethyl-6-(1-methyl-1-phenyl-ethyl)-1,4-dioxa-spiro[4.5]decan-2-one

A: 7699-00-5
(R)-Ethyl lactate

B: 97371-54-5
(-)-(2S,5R)-5-Methyl-2-(1-methyl-1-phenylethyl)cyclohexanon

Conditions

Conditions	Yield
With hydrogenchloride for 2h; Heating;	A 84% B n/a

...Expand

: 617-35-6
2-oxo-propionic acid ethyl ester

A: 687-47-8
(S)-Ethyl lactate

B: 7699-00-5
(R)-Ethyl lactate

Conditions

Conditions	Yield
With hydrogen; cinchonidine In cyclohexane at 24.84℃; under 30003 Torr; optical yield given as %ee; enantioselective reaction;	A n/a B 76%
With D-Glucose; cliona varians In water at 25℃; for 72h; Reagent/catalyst;	A 49% B n/a
With hydrogen; cinchonine; Pt/Al2O3 In toluene at 20℃; under 15001.2 Torr; Rate constant; Product distribution; var. conc. of HCd, solvent;

: 64-17-5
ethanol

: 13076-17-0
D-lactide

: 7699-00-5
(R)-Ethyl lactate

Conditions

Conditions	Yield
With hydrogenchloride In toluene	76%

: 617-35-6
2-oxo-propionic acid ethyl ester

: 7699-00-5
(R)-Ethyl lactate

Conditions

Conditions	Yield
With glycerol dehydrogenase; 2-propanol-NAD(1+) potassium phosphate buffer, pH 7;	61%
With Leifsonia sp. S749 cells alcohol dehydrogenase; nicotinamide adenine dinucleotide; isopropyl alcohol In phosphate buffer at 25℃; for 24h; pH=7.0;	19%
With hydrogen; (R)-N-<2-hydroxy2-(1-naphthyl)ethyl>pyrrolidine; Pt/Al2O3 In acetic acid at 25℃; under 7500.6 Torr; for 2h; Product distribution; enantioselectivity; var. modifiers, also in the absence of modifiers, var. solvents, temp., pressure and time;

: 64-17-5
ethanol

: 18668-00-3
(R)-(+)-2-acetoxypropionic acid

: 7699-00-5
(R)-Ethyl lactate

Conditions

Conditions	Yield
With sulfuryl dichloride at -40 - 20℃; for 48h;	58%

: 97-64-3, 2676-33-7
ethyl 2-hydroxypropionate

A: 79-33-4
L-Lactic acid

B: 10326-41-7
D-Lactic acid

C: 7699-00-5
(R)-Ethyl lactate

Conditions

Conditions	Yield
With ammonium hydroxide at 30℃; pH=6.9;	A n/a B n/a C 34.5%

...Expand

: 997-04-6
2-nitryloxy-propionic acid ethyl ester

A: 687-47-8
(S)-Ethyl lactate

B: 7699-00-5
(R)-Ethyl lactate

Conditions

Conditions	Yield
With acetic acid; zinc Yield given. Yields of byproduct given. Title compound not separated from byproducts;

: 20918-92-7
(R)-2-(Acetoxy)propionsaeure-ethylester

: 7699-00-5
(R)-Ethyl lactate

Conditions

Conditions	Yield
With toluene-4-sulfonic acid In ethanol for 72h; Heating; Yield given;

: 90246-32-5
(1R)-2-ethoxy-1-methyl-2-oxoethyl 4-nitrobenzoate

: 7699-00-5
(R)-Ethyl lactate

Conditions

Conditions	Yield
With potassium carbonate In ethanol at 23℃; for 15h;

: 64-17-5
ethanol

: 17392-83-5
(R)-Methyl lactate

: 7699-00-5
(R)-Ethyl lactate

Conditions

Conditions	Yield
With toluene-4-sulfonic acid for 30h; Heating; Yield given;

: 97-64-3, 2676-33-7
ethyl 2-hydroxypropionate

: 160289-70-3
(R)-(1-naphthyl)-glycyl-(R)-phenylglycine

A: 7699-00-5
(R)-Ethyl lactate

B: (R)-((R)-2-Amino-2-naphthalen-1-yl-acetylamino)-phenyl-acetic acid; compound with (S)-2-hydroxy-propionic acid ethyl ester

C: (R)-((R)-2-Amino-2-naphthalen-1-yl-acetylamino)-phenyl-acetic acid; compound with (R)-2-hydroxy-propionic acid ethyl ester

Conditions

Conditions	Yield
In methanol Ambient temperature; Yield given; Title compound not separated from byproducts;

...Expand

: 10009-70-8
R-(+)-2-bromopropionic acid

: 7732-18-5
water

Ag2O: Ag2O

: 7699-00-5
(R)-Ethyl lactate

Conditions

Conditions	Yield
anschliessende Veresterung;

...Expand

: 10009-70-8
R-(+)-2-bromopropionic acid

: 67-64-1
acetone

Ag2O: Ag2O

: 7699-00-5
(R)-Ethyl lactate

Conditions

Conditions	Yield
anschliessende Veresterung;

...Expand

: 64-17-5
ethanol

calcium salt of/the/ d(-)-lactic acid: calcium salt of/the/ d(-)-lactic acid

: 7699-00-5
(R)-Ethyl lactate

Conditions

Conditions	Yield
With sulfuric acid

: 10009-70-8
R-(+)-2-bromopropionic acid

: silver nitrate

diluted HNO3: diluted HNO3

: 7699-00-5
(R)-Ethyl lactate

Conditions

Conditions	Yield
at 50℃; anschliessende Veresterung;

...Expand

: 75-03-6
ethyl iodide

silver salt of/the/ l-lactic acid: silver salt of/the/ l-lactic acid

: 7699-00-5
(R)-Ethyl lactate

: 80-40-0
ethyl ester of p-toluenesulfonic acid

sodium salt of/the/ d(-)-lactic acid: sodium salt of/the/ d(-)-lactic acid

: 7699-00-5
(R)-Ethyl lactate

Conditions

Conditions	Yield
With ethanol

: 64-17-5
ethanol

zinc ammonium salt of/the/ d(-)-lactic acid: zinc ammonium salt of/the/ d(-)-lactic acid

: 7699-00-5
(R)-Ethyl lactate

Conditions

Conditions	Yield
With sulfuric acid

: 687-47-8
(S)-Ethyl lactate

A: 7699-00-5
(R)-Ethyl lactate

B inactive lactic acid ethyl ester: inactive lactic acid ethyl ester

Conditions

Conditions	Yield
durch Schweineleber-Lipase schneller gespalten;

: 64-17-5
ethanol

l(-)-p-toluenesulfonyl-lactic acid ethyl ester: l(-)-p-toluenesulfonyl-lactic acid ethyl ester

A: 7699-00-5
(R)-Ethyl lactate

B levorotatory O-ethyllactic acid ethyl ester: levorotatory O-ethyllactic acid ethyl ester

Conditions

Conditions	Yield
With potassium carbonate

...Expand

: 56985-74-1, 112449-57-7, 112529-73-4
(R)-2-bromo-propionic acid ; sodium salt

Ag2O: Ag2O

water: water

: 7699-00-5
(R)-Ethyl lactate

Conditions

Conditions	Yield
at 0℃; anschliessende Veresterung sowie Hydrolyse-geschwindigkeiten;

...Expand

: 617-35-6
2-oxo-propionic acid ethyl ester

: 67-56-1
methanol

A: 547-64-8
methyl lactate

B: 687-47-8
(S)-Ethyl lactate

C: 7699-00-5
(R)-Ethyl lactate

Conditions

Conditions	Yield
With hydrogen; chiral Ru complex at 20℃; under 25857.4 Torr; for 48h; Product distribution; Further Variations:; Catalysts; Temperatures; Solvents;

...Expand

: 64-17-5
ethanol

: 3,6-dimethyl-1,4-dioxane-2,5-dione

A: 7699-00-5
(R)-Ethyl lactate

B: 64231-47-6
(S)-2-hydroxy-propionic acid (S)- 1-ethoxycarbonyl-ethyl ester

Conditions

Conditions	Yield
With Candida antarctica lipase B In tetrahydrofuran; hexane at 60℃; for 66h;	A 49 % Chromat. B 48 % Chromat.

...Expand

: 687-47-8
(S)-Ethyl lactate

: 7699-00-5
(R)-Ethyl lactate

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 1) Ph3P, diethyl azodicarboxylate / 2) THF, -20 deg C, 0.5 h, 2) THF, 27 h 2: K2CO3 / ethanol / 15 h / 23 °C View Scheme
Multi-step reaction with 3 steps 1: 87 percent / pyridine / 3 h / 0 - 10 °C 2: 85 percent / dimethylsulfoxide / 12 h 3: 4-toluenesulfonic acid / ethanol / 72 h / Heating View Scheme

: 57057-80-4
ethyl (S)-2-[[(4-methylphenyl)sulfonyl]oxy]propanoate

: 7699-00-5
(R)-Ethyl lactate

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 85 percent / dimethylsulfoxide / 12 h 2: 4-toluenesulfonic acid / ethanol / 72 h / Heating View Scheme

: 63696-99-1
(S)-ethyl 2-(methylsulfonyloxy)propanoate

: 7699-00-5
(R)-Ethyl lactate

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 90 percent / Amberlyst A-26 NO3(1-) form / pentane / 5 h / 120 °C 2: Zn, CH3COOH View Scheme

: C18H20O3

A: 687-47-8
(S)-Ethyl lactate

B: 7699-00-5
(R)-Ethyl lactate

Conditions

Conditions	Yield
With methanol; toluene-4-sulfonic acid Inert atmosphere; optical yield given as %ee;
With toluene-4-sulfonic acid In methanol Inert atmosphere; optical yield given as %ee;

: 617-35-6
2-oxo-propionic acid ethyl ester

: 15206-55-0
methyl 2-oxo-2-phenylacetate

A: 687-47-8
(S)-Ethyl lactate

B: 7699-00-5
(R)-Ethyl lactate

C: 21210-43-5
(S)-Methyl mandelate

D: 20698-91-3
(R)-methyl mandelate

Conditions

Conditions	Yield
With 5% Pt/Al2O3; hydrogen; acetic acid In toluene at 19.84℃; under 30003 Torr;

...Expand

: 7699-00-5
(R)-Ethyl lactate

: 18162-48-6
tert-butyldimethylsilyl chloride

: (R)-ethyl 2-((tert-butyldimethylsilyl)oxy)propanoate

Conditions

Conditions	Yield
With 1H-imidazole In dichloromethane	99%
With 1H-imidazole In dichloromethane at 0 - 20℃; for 3h;	99%
With 1H-imidazole In dichloromethane at 20℃; for 4h; Inert atmosphere;	96%
With 1H-imidazole In N,N-dimethyl-formamide at 25℃; Etherification;
With 1H-imidazole In dichloromethane at 0 - 20℃; for 5h;

: 7699-00-5
(R)-Ethyl lactate

: 28917-43-3
3,5-dibenzyloxybenzoic acid

: (S)-1-ethoxy-1-oxopropan-2-yl 3,5-bis(benzyloxy)benzoate

Conditions

Conditions	Yield
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran at 20℃; for 3h; Inert atmosphere;	99%

: 7699-00-5
(R)-Ethyl lactate

: 75-03-6
ethyl iodide

: 869588-04-5
ethyl (R)-2-ethoxypropanoate

Conditions

Conditions	Yield
With silver(l) oxide In diethyl ether at 23 - 42℃; Williamson Ether Synthesis; Reflux;	98%
With silver(l) oxide

: 7699-00-5
(R)-Ethyl lactate

: 4254-14-2
(2R)-propane-1,2-diol

Conditions

Conditions	Yield
With lithium aluminium tetrahydride In diethyl ether for 0.5h; Heating;	97%
With sodium tetrahydroborate; aluminium trichloride

: 7699-00-5
(R)-Ethyl lactate

: 124-63-0
methanesulfonyl chloride

: 63696-99-1
(S)-ethyl 2-(methylsulfonyloxy)propanoate

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 0℃;	95%

: 7699-00-5
(R)-Ethyl lactate

: 36112-61-5
6-methoxy-1-naphthoic acid

: (R)-[1-ethoxy-1-carbonylpropan-2-yl]-6-methoxy-1-naphthoic acid ester

Conditions

Conditions	Yield
Stage #1: 6-methoxy-1-naphthoic acid With thionyl chloride In N,N-dimethyl-formamide; toluene at 10 - 40℃; for 4h; Green chemistry; Stage #2: (R)-Ethyl lactate With triethylamine In toluene at 10 - 20℃; for 2h; Green chemistry;	92%

: 7699-00-5
(R)-Ethyl lactate

: 108-95-2
phenol

: 76671-56-2
(R)-2-phenoxypropionic acid ethyl ester

Conditions

Conditions	Yield
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran; toluene at 0 - 20℃; Mitsunobu reaction; Inert atmosphere;	91%
With di-tert-butyl-diazodicarboxylate; triphenylphosphine In tetrahydrofuran Mitsunobu Displacement;

: 7699-00-5
(R)-Ethyl lactate

: 13154-24-0
triisopropylsilyl chloride

: ethyl (R)-2-((triisopropylsilyl)oxy)propanoate

Conditions

Conditions	Yield
With 1H-imidazole In N,N-dimethyl-formamide at 0 - 20℃; for 12h; Inert atmosphere;	91%

: 7699-00-5
(R)-Ethyl lactate

: 108-46-3
recorcinol

: diethyl (2R,2'R)-2,2'-(1,3-phenylene)bis(oxy)dipropanoate

Conditions

Conditions	Yield
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran; toluene at 0 - 20℃; Mitsunobu reaction; Inert atmosphere;	90%

: 7699-00-5
(R)-Ethyl lactate

: 100865-93-8
O-diphenylmethyl 2,2,2-trichloroacetimidate

: (R)-ethyl 2-(benzhydryloxy)propanoate

Conditions

Conditions	Yield
In toluene at 111℃;	90%

: 7699-00-5
(R)-Ethyl lactate

: 86-55-5
1-naphthalenecarboxylic acid

: (R)-[1-ethoxy-1-carbonylpropan-2-yl]-1-naphthoic acid ester

Conditions

Conditions	Yield
Stage #1: 1-naphthalenecarboxylic acid With thionyl chloride In N,N-dimethyl-formamide; toluene at 10 - 40℃; for 4h; Green chemistry; Stage #2: (R)-Ethyl lactate With triethylamine In toluene at 10 - 20℃; for 2h; Green chemistry;	90%

: 7699-00-5
(R)-Ethyl lactate

: 41046-67-7
2-iodoresorcinol

: 1226896-32-7
(2R,2'R)-diethyl 2,2'-(2-iodo-1,3-phenylene)bis(oxy)dipropanoate

Conditions

Conditions	Yield
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran; toluene at 0 - 20℃; for 6h;	90%

: 7699-00-5
(R)-Ethyl lactate

: 84028-88-6
ethyl (S)-lactate triflate

: 171753-75-6
R,R-dilactic acid diethyl ester

Conditions

Conditions	Yield
With potassium carbonate In 1,2-dichloro-ethane; pentane at 20℃; for 24h;	89%
With potassium carbonate In 1,2-dichloro-ethane; pentane at 20℃; for 48h; Inert atmosphere;	20%

: 7699-00-5
(R)-Ethyl lactate

: 171414-16-7
N-(4-methoxybenzyl)-2-nitro-N-(prop-2-yn-1-yl)benzenesulfonamide

: (R)-2-[(4-Methoxy-benzyl)-(2-nitro-benzenesulfonyl)-amino]-propionic acid ethyl ester

Conditions

Conditions	Yield
With triphenylphosphine; diethylazodicarboxylate In dichloromethane at 23℃; for 1h;	87%

: 7699-00-5
(R)-Ethyl lactate

: 111-83-1
1-bromo-octane

: 103117-91-5
(2R)-3-octylundecane-2,3-diol

Conditions

Conditions	Yield
With magnesium In tetrahydrofuran for 1.5h; Ambient temperature;	86%

: 150-19-6
O-methylresorcine

: 7699-00-5
(R)-Ethyl lactate

: ethyl (R)-2-(3-methoxyphenoxy)propanoate

Conditions

Conditions	Yield
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran; toluene at 0 - 20℃; Mitsunobu reaction; Inert atmosphere;	86%

: 7699-00-5
(R)-Ethyl lactate

: 98-59-9
p-toluenesulfonyl chloride

: 117589-34-1
(-)-ethyl 2-<(p-tolylsulfonyl)oxy>propionate

Conditions

Conditions	Yield
With triethylamine In benzene for 6h; Ambient temperature;	85.1%
With pyridine Substitution;	85%
Stage #1: (R)-Ethyl lactate; p-toluenesulfonyl chloride In dichloromethane at 0 - 10℃; for 0.166667h; Inert atmosphere; Stage #2: With triethylamine In dichloromethane at 20℃; for 4h; Cooling;	85.1%

: 7699-00-5
(R)-Ethyl lactate

: 2-(benzyloxy)-4-bromophenol

: (2S)-methyl 2-(2-(benzyloxy)-4-bromophenoxy)propanoate

Conditions

Conditions	Yield
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran at 0 - 20℃; for 4h; Mitsunobu Displacement; Inert atmosphere;	85%

: 7699-00-5
(R)-Ethyl lactate

: 120-83-2
2,4-dichlorophenol

: 66423-06-1
(R)-2-(2,4-Dichlorphenoxy)propionsaeure-ethylester

Conditions

Conditions	Yield
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran at 20℃; for 16h; Mitsunobu Displacement;	84%
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran Mitsunobu reaction;

: 674-82-8
4-methyleneoxetan-2-one

: 7699-00-5
(R)-Ethyl lactate

: 143444-49-9
(R)-1-ethoxy-1-oxopropan-2-yl 3-oxobutanoate

Conditions

Conditions	Yield
With triethylamine In dichloromethane for 15h; Heating;	81%

: 7699-00-5
(R)-Ethyl lactate

: 62-23-7
4-nitro-benzoic acid

: ethyl (S)-2-((4-nitrobenzoyl)oxy)propanoate

Conditions

Conditions	Yield
With PPh3-containing polystyrene non-cross-linked polymer; diethylazodicarboxylate In tetrahydrofuran at 20℃; for 0.5h; Mitsunobu reaction;	80%

: 7699-00-5
(R)-Ethyl lactate

: 1-chloro-N-(2,6-dichlorophenyl)methanesulfonamide

: ethyl (2S)-2-[2,6-dichloro-N-(chloromethylsulfonyl)anilino]propanoate

Conditions

Conditions	Yield
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran at 0 - 20℃;	79%

: 7699-00-5
(R)-Ethyl lactate

: 74-11-3
para-chlorobenzoic acid

: 1259030-71-1
(R)-1-ethoxy-1-oxopropane-2-yl 4-chlorobenzoate

Conditions

Conditions	Yield
With C18H20N2O4; Nb-TPP In tetrahydrofuran at 0 - 20℃; Mitsunobu reaction;	76%

: 7699-00-5
(R)-Ethyl lactate

: 62-23-7
4-nitro-benzoic acid

: 90246-32-5
(1R)-2-ethoxy-1-methyl-2-oxoethyl 4-nitrobenzoate

Conditions

Conditions	Yield
With C18H20N2O4; Nb-TPP In tetrahydrofuran at 0 - 20℃; Mitsunobu reaction;	74%
With 1-phenylphospholane-1-oxide; di-isopropyl azodicarboxylate; phenylsilane In tetrahydrofuran at 80℃; for 18h; Mitsunobu Displacement; Sealed tube;	68%

: 7699-00-5
(R)-Ethyl lactate

: (S)-ethyl 2-(2-hydroxyphenoxy)propanoate

: C16H22O6

Conditions

Conditions	Yield
With di-isopropyl azodicarboxylate; triphenylphosphine In toluene at 0 - 20℃; Mitsunobu Displacement;	74%

: 7699-00-5
(R)-Ethyl lactate

: 99-64-9
3-(dimethylamino)benzoic acid

: 1259030-70-0
(R)-1-ethoxy-1-oxopropan-2-yl 3-(dimethylamino)benzoate

Conditions

Conditions	Yield
With C18H20N2O4; Nb-TPP In tetrahydrofuran at 0 - 20℃; Mitsunobu reaction;	73%

Propanoicacid, 2-hydroxy-, ethyl ester, (2R)- Specification

The Propanoicacid, 2-hydroxy-, ethyl ester, (2R)-, with the CAS registry number 7699-00-5, has the systematic name of ethyl 2-hydroxypropanoate. It belongs to the product category of Acetyl Group. And the molecular formula of the chemical is C₅H₁₀O₃.

The characteristics of Propanoicacid, 2-hydroxy-, ethyl ester, (2R)- are as followings: (1)# of Rule of 5 Violations: 0; (2)ACD/BCF (pH 5.5): 1; (3)ACD/BCF (pH 7.4): 1; (4)ACD/KOC (pH 5.5): 18.84; (5)ACD/KOC (pH 7.4): 18.84; (6)#H bond acceptors: 3; (7)#H bond donors: 1; (8)#Freely Rotating Bonds: 4; (9)Polar Surface Area: 46.53 Å²; (10)Index of Refraction: 1.42; (11)Molar Refractivity: 28.48 cm³; (12)Molar Volume: 112.4 cm³; (13)Polarizability: 11.29×10^-24cm³; (14)Surface Tension: 33.2 dyne/cm; (15)Density: 1.05 g/cm³; (16)Flash Point: 54.6 °C; (17)Enthalpy of Vaporization: 45.57 kJ/mol; (18)Boiling Point: 154.5 °C at 760 mmHg; (19)Vapour Pressure: 1.16 mmHg at 25°C.

You should be cautious while dealing with this chemical. It is a kind of flammable chemical which irritates to respiratory system. What's more, it has risk of serious damage to eyes. Therefore, you had better take the following instructions: Avoid contact with skin; Wear eye/face protection, and if in case of contact with eyes, rinse immediately with plenty of water and seek medical advice.

Addtionally, the following datas could be converted into the molecular structure:
(1)SMILES: CCOC(=O)C(C)O
(2)InChI: InChI=1/C5H10O3/c1-3-8-5(7)4(2)6/h4,6H,3H2,1-2H3
(3)InChIKey: LZCLXQDLBQLTDK-UHFFFAOYAV

Product Name

(+)-ETHYL D-LACTATE

Synthetic route

Propanoicacid, 2-hydroxy-, ethyl ester, (2R)- Specification

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