Product Name

  • Name

    L-Alaninamide hydrochloride

  • EINECS 608-843-1
  • CAS No. 33208-99-0
  • Article Data6
  • CAS DataBase
  • Density
  • Solubility
  • Melting Point 212-217 °C
  • Formula C3H8N2O.HCl
  • Boiling Point 247.4 °C at 760 mmHg
  • Molecular Weight 124.57
  • Flash Point 103.4 °C
  • Transport Information
  • Appearance white to light yellow crystal powder
  • Safety 24/25
  • Risk Codes
  • Molecular Structure Molecular Structure of 33208-99-0 (L-Alaninamide hydrochloride)
  • Hazard Symbols CorrosiveC
  • Synonyms L-Alanine amide hydrochloride;H-ALA-NH2.HCL;Propanamide, 2-amino-, monohydrochloride, (2S)-(9CI);Propanamide, 2-amino-, monohydrochloride, (S)-;(2S)-2-Aminopropanamide hydrochloride;Alanine amide hydrochloride;
  • PSA 69.11000
  • LogP 1.02150

Synthetic route

rac-Ala-OH
302-72-7

rac-Ala-OH

A

(S)-alaninamide hydrochloride
33208-99-0

(S)-alaninamide hydrochloride

B

D-alaninamide hydrochloride
71810-97-4

D-alaninamide hydrochloride

Conditions
ConditionsYield
With laccase; ammonia In water at 38 - 40℃; Temperature; Enzymatic reaction;A 92%
B n/a
tert-butyl (1S)-2-amino-1-methyl-2-oxoethylcarbamate
78981-25-6, 81587-17-9, 85642-13-3

tert-butyl (1S)-2-amino-1-methyl-2-oxoethylcarbamate

(S)-alaninamide hydrochloride
33208-99-0

(S)-alaninamide hydrochloride

Conditions
ConditionsYield
With acetyl chloride In ethanol; ethyl acetate for 1h;80%
With hydrogenchloride In 1,4-dioxane at 80℃; for 4h;
L-alanine methyl ester hydrochloride
2491-20-5

L-alanine methyl ester hydrochloride

(S)-alaninamide hydrochloride
33208-99-0

(S)-alaninamide hydrochloride

Conditions
ConditionsYield
With ammonia In methanol for 72h; Ambient temperature;
Stage #1: L-alanine methyl ester hydrochloride With ammonia at 20℃; for 20h; Sealed tube; Large scale;
Stage #2: With hydrogenchloride In water pH=1.55; pH-value; Large scale;		85 g
3-Phenylbutyraldehyde
16251-77-7

3-Phenylbutyraldehyde

(S)-alaninamide hydrochloride
33208-99-0

(S)-alaninamide hydrochloride

(5S)-5-methyl-2-(2-phenylpropyl)imidazolidin-4-one
1084907-53-8

(5S)-5-methyl-2-(2-phenylpropyl)imidazolidin-4-one

Conditions
ConditionsYield
With potassium carbonate; triethylamine In ethanol at 60℃; for 24h;100%
With potassium carbonate; triethylamine In ethanol at 60℃; for 24h; Inert atmosphere;100%
AbzBB-OPfp

AbzBB-OPfp

(S)-alaninamide hydrochloride
33208-99-0

(S)-alaninamide hydrochloride

(2S)-2-(4-hydroxy-2-oxo-1,4-dihydroquinazolin-3(2H)-yl)propanamide

(2S)-2-(4-hydroxy-2-oxo-1,4-dihydroquinazolin-3(2H)-yl)propanamide

Conditions
ConditionsYield
With N-ethylmorpholine; In N,N-dimethyl-formamide at 20℃;100%
(S)-alaninamide hydrochloride
33208-99-0

(S)-alaninamide hydrochloride

(2S,2'S)-4,4'-disulfanediylbis(2-(tert-butoxycarbonyl)amino)butanoic acid
130981-51-0

(2S,2'S)-4,4'-disulfanediylbis(2-(tert-butoxycarbonyl)amino)butanoic acid

(Boc-Hcy-Ala-NH2)2
569341-03-3

(Boc-Hcy-Ala-NH2)2

Conditions
ConditionsYield
With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; for 5h;99%
BOC-L-aspartic acid 4-benzyl ester
7536-58-5

BOC-L-aspartic acid 4-benzyl ester

(S)-alaninamide hydrochloride
33208-99-0

(S)-alaninamide hydrochloride

BOC-Asp(OBn)-Ala-NH2
302911-12-2

BOC-Asp(OBn)-Ala-NH2

Conditions
ConditionsYield
Stage #1: BOC-L-aspartic acid 4-benzyl ester With 4-methyl-morpholine; isobutyl chloroformate In tetrahydrofuran; N,N-dimethyl-formamide at -40 - 0℃; for 1h;
Stage #2: (S)-alaninamide hydrochloride With 4-methyl-morpholine In tetrahydrofuran; N,N-dimethyl-formamide at 20℃; for 24h;		99%
3-((quinoline-8-oxy)methyl)benzaldehyde

3-((quinoline-8-oxy)methyl)benzaldehyde

(S)-alaninamide hydrochloride
33208-99-0

(S)-alaninamide hydrochloride

(S)-2-((3-((quinolin-8-yloxy)methyl)benzyl)amino)propanamide

(S)-2-((3-((quinolin-8-yloxy)methyl)benzyl)amino)propanamide

Conditions
ConditionsYield
Stage #1: (S)-alaninamide hydrochloride With triethylamine In methanol at 20℃; for 0.5h;
Stage #2: 3-((quinoline-8-oxy)methyl)benzaldehyde In methanol at 20℃; for 2h;
Stage #3: With potassium borohydride In methanol for 3h; Reflux;		96.08%
Stage #1: (S)-alaninamide hydrochloride With triethylamine In methanol at 20℃; for 1h;
Stage #2: 3-((quinoline-8-oxy)methyl)benzaldehyde In methanol for 2h;
Stage #3: With potassium borohydride In methanol for 3h; Reflux;		96%
benzyloxycarbonyl-L-leucine benzyl ester
124980-31-0

benzyloxycarbonyl-L-leucine benzyl ester

(S)-alaninamide hydrochloride
33208-99-0

(S)-alaninamide hydrochloride

Cbz-Leu-Ala-NH2
62074-75-3

Cbz-Leu-Ala-NH2

Conditions
ConditionsYield
With Alcalase In tert-Amyl alcohol at 5℃; for 96h; Condensation;96%
N-α-tert-butyloxycarbonyl-N-ε-benzyloxycarbonyl-lysine p-nitrophenyl ester
2389-46-0

N-α-tert-butyloxycarbonyl-N-ε-benzyloxycarbonyl-lysine p-nitrophenyl ester

(S)-alaninamide hydrochloride
33208-99-0

(S)-alaninamide hydrochloride

Nα-BOC-Nε-CBZ-L-lysyl-L-alanine amide
163848-14-4

Nα-BOC-Nε-CBZ-L-lysyl-L-alanine amide

Conditions
ConditionsYield
With triethylamine In ethyl acetate; N,N-dimethyl-formamide96%
2,2,2-trifluoroethyl chloroformate
27746-99-2

2,2,2-trifluoroethyl chloroformate

(S)-alaninamide hydrochloride
33208-99-0

(S)-alaninamide hydrochloride

N-(2,2,2-trifluoroethoxycarbonyl)-L-alaninamide
951242-82-3

N-(2,2,2-trifluoroethoxycarbonyl)-L-alaninamide

Conditions
ConditionsYield
With sodium hydrogencarbonate In water; ethyl acetate at 20℃; for 2.5h;95%
3-chloro-5-(trifluoromethyl)benzoic acid
53985-49-2

3-chloro-5-(trifluoromethyl)benzoic acid

(S)-alaninamide hydrochloride
33208-99-0

(S)-alaninamide hydrochloride

N-[(2S)-1-amino-1-oxopropan-2-yl]-3-chloro-5-(trifluoromethyl)benzamide

N-[(2S)-1-amino-1-oxopropan-2-yl]-3-chloro-5-(trifluoromethyl)benzamide

Conditions
ConditionsYield
With 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; triethylamine In ethyl acetate; N,N-dimethyl-formamide for 0.5h;95%
1,5-difluoro-2,4-dinitrobenzene
327-92-4

1,5-difluoro-2,4-dinitrobenzene

(S)-alaninamide hydrochloride
33208-99-0

(S)-alaninamide hydrochloride

N-(2,4-dinitro-5-fluorophenyl)-L-alaninamide

N-(2,4-dinitro-5-fluorophenyl)-L-alaninamide

Conditions
ConditionsYield
Stage #1: (S)-alaninamide hydrochloride With magnesium sulfate; sodium hydroxide In water; acetone at 20℃; for 4h;
Stage #2: 1,5-difluoro-2,4-dinitrobenzene In water; acetone at 1℃; for 20h;		93%
Stage #1: (S)-alaninamide hydrochloride With magnesium sulfate; sodium hydroxide In acetone at 20℃; for 3h;
Stage #2: 1,5-difluoro-2,4-dinitrobenzene In acetone for 0.5h;		63%
5-benzyloxyindole-3-carboxaldehyde
6953-22-6

5-benzyloxyindole-3-carboxaldehyde

(S)-alaninamide hydrochloride
33208-99-0

(S)-alaninamide hydrochloride

(S)-2-((5-(benzyloxy)-1H-indol-3-yl)methylamino)propanamide

(S)-2-((5-(benzyloxy)-1H-indol-3-yl)methylamino)propanamide

Conditions
ConditionsYield
Stage #1: (S)-alaninamide hydrochloride With sodium cyanoborohydride In methanol at 20℃; for 0.25h; Molecular sieve; Inert atmosphere;
Stage #2: 5-benzyloxyindole-3-carboxaldehyde In methanol at 20 - 35℃; for 4h; Inert atmosphere;		92.1%
4-((2-fluorobenzyl)oxy)benzaldehyde
70627-20-2

4-((2-fluorobenzyl)oxy)benzaldehyde

(S)-alaninamide hydrochloride
33208-99-0

(S)-alaninamide hydrochloride

ralfinamide

ralfinamide

Conditions
ConditionsYield
Stage #1: (S)-alaninamide hydrochloride With triethylamine In methanol at 20℃;
Stage #2: 4-((2-fluorobenzyl)oxy)benzaldehyde In methanol at 25℃; for 3.33333h;
Stage #3: With sodium hydroxide; sodium tetrahydroborate In methanol; water at 8℃; for 4h; Product distribution / selectivity;		92%
Stage #1: 4-((2-fluorobenzyl)oxy)benzaldehyde; (S)-alaninamide hydrochloride With triethylamine In methanol at 20 - 25℃; for 1h;
Stage #2: With hydrogen; 5 % platinum on carbon In methanol at 20 - 35℃; under 3750.38 Torr; for 5h; Product distribution / selectivity;		85%
Stage #1: 4-((2-fluorobenzyl)oxy)benzaldehyde; (S)-alaninamide hydrochloride With triethylamine In methanol at 20 - 25℃; for 1h;
Stage #2: With hydrogen; palladium 10% on activated carbon In methanol at 20 - 35℃; under 3750.38 Torr; for 5h; Product distribution / selectivity;		70%
(S)-alaninamide hydrochloride
33208-99-0

(S)-alaninamide hydrochloride

N,N'-disuccinimidyl-2,2'-dithiosalicylate
497262-13-2

N,N'-disuccinimidyl-2,2'-dithiosalicylate

N,N'-(2,2'-dithiobisbenzoyl)-bis-L-alaninamide
449775-52-4

N,N'-(2,2'-dithiobisbenzoyl)-bis-L-alaninamide

Conditions
ConditionsYield
With triethylamine In N,N-dimethyl-formamide at 20℃;92%
With triethylamine In N,N-dimethyl-formamide at 25℃;
(S)-alaninamide hydrochloride
33208-99-0

(S)-alaninamide hydrochloride

(S)-6-trifluoroacetylamino-2-(tert-butoxycarbonylamino)-hexanoic acid
96561-04-5, 16965-06-3

(S)-6-trifluoroacetylamino-2-(tert-butoxycarbonylamino)-hexanoic acid

Boc-L-Lys(COCF3)-L-Ala-NH2
1382351-57-6

Boc-L-Lys(COCF3)-L-Ala-NH2

Conditions
ConditionsYield
With cyano-hydroxyimino-acetic acid 2,2-dimethyl-[1,3]dioxolan-4-ylmethyl ester; sodium hydrogencarbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In water at 20℃; for 2h; optical yield given as %de;92%
1-bromomethyl o-carborane

1-bromomethyl o-carborane

(S)-alaninamide hydrochloride
33208-99-0

(S)-alaninamide hydrochloride

C6H21B10N2O

C6H21B10N2O

Conditions
ConditionsYield
With 1-butyl-2,3-dimethylimidazolium tetrafluoroborate; triethylamine at 60 - 70℃; for 6h; Reagent/catalyst;92%
4-((2,3-dihydrobenzo[b]thiophen-7-oxy)methyl)benzaldehyde

4-((2,3-dihydrobenzo[b]thiophen-7-oxy)methyl)benzaldehyde

(S)-alaninamide hydrochloride
33208-99-0

(S)-alaninamide hydrochloride

(S)-2-(4-((2,3-dihydrobenzo[b]thiophen-7-oxy)methyl)benzylamino)propanamide

(S)-2-(4-((2,3-dihydrobenzo[b]thiophen-7-oxy)methyl)benzylamino)propanamide

Conditions
ConditionsYield
Stage #1: (S)-alaninamide hydrochloride With triethylamine In methanol at 20℃; for 0.5h;
Stage #2: 4-((2,3-dihydrobenzo[b]thiophen-7-oxy)methyl)benzaldehyde In methanol at 20℃; for 2h;
Stage #3: With potassium borohydride In methanol for 3h; Reflux;		91.67%
3-((benzofuran-4-oxy)methyl) benzaldehyde

3-((benzofuran-4-oxy)methyl) benzaldehyde

(S)-alaninamide hydrochloride
33208-99-0

(S)-alaninamide hydrochloride

(S)-2-((3-((benzofuran-4-yloxy)methyl)benzyl)amino)propanamide

(S)-2-((3-((benzofuran-4-yloxy)methyl)benzyl)amino)propanamide

Conditions
ConditionsYield
Stage #1: (S)-alaninamide hydrochloride With triethylamine In methanol at 20℃; for 1h;
Stage #2: 3-((benzofuran-4-oxy)methyl) benzaldehyde In methanol at 20℃; for 2h;
Stage #3: With potassium borohydride In methanol for 3h; Reflux;		91.18%
Stage #1: (S)-alaninamide hydrochloride With triethylamine In methanol at 20℃; for 1h;
Stage #2: 3-((benzofuran-4-oxy)methyl) benzaldehyde In methanol for 2h;
Stage #3: With potassium borohydride In methanol for 3h; Reflux;		91%
Cbz-Tyr-OH
1164-16-5

Cbz-Tyr-OH

(S)-alaninamide hydrochloride
33208-99-0

(S)-alaninamide hydrochloride

Z-Tyr-Ala-NH2
35807-79-5

Z-Tyr-Ala-NH2

Conditions
ConditionsYield
With sodium hydroxide; δ-chymotrypsin In hydrogenchloride for 168h; Ambient temperature;91%
4-((benzofuran-4-oxy)methyl)benzaldehyde

4-((benzofuran-4-oxy)methyl)benzaldehyde

(S)-alaninamide hydrochloride
33208-99-0

(S)-alaninamide hydrochloride

(S)-2-((4-((benzofuran-4-yloxy)methyl)benzyl)amino)propanamide

(S)-2-((4-((benzofuran-4-yloxy)methyl)benzyl)amino)propanamide

Conditions
ConditionsYield
Stage #1: (S)-alaninamide hydrochloride With triethylamine In methanol at 20℃; for 1h;
Stage #2: 4-((benzofuran-4-oxy)methyl)benzaldehyde In methanol for 2h;
Stage #3: With potassium borohydride In methanol for 3h; Reflux;		91%
Stage #1: (S)-alaninamide hydrochloride With triethylamine In methanol at 20℃; for 1h;
Stage #2: 4-((benzofuran-4-oxy)methyl)benzaldehyde In methanol at 20℃; for 2h;
Stage #3: With potassium borohydride In methanol for 3h; Reflux;		55.91%
di-tert-butyl dicarbonate
24424-99-5

di-tert-butyl dicarbonate

(S)-alaninamide hydrochloride
33208-99-0

(S)-alaninamide hydrochloride

tert-butyl (1S)-2-amino-1-methyl-2-oxoethylcarbamate
78981-25-6, 81587-17-9, 85642-13-3

tert-butyl (1S)-2-amino-1-methyl-2-oxoethylcarbamate

Conditions
ConditionsYield
With triethylamine In methanol for 12h;90%
With triethylamine In dichloromethane for 3h;74%
With triethylamine In tetrahydrofuran; water at 20℃; for 16h;73%
With triethylamine In tetrahydrofuran; water at 20℃; for 16h;73%
With sodium carbonate In 1,4-dioxane; water for 15h;
(S)-alaninamide hydrochloride
33208-99-0

(S)-alaninamide hydrochloride

p-methoxybenzyloxycarbonyl-Phe-OMe
97985-98-3

p-methoxybenzyloxycarbonyl-Phe-OMe

Moz-Phe-Ala-NH2
145126-20-1

Moz-Phe-Ala-NH2

Conditions
ConditionsYield
With Alcalase In tert-Amyl alcohol at 5℃; for 48h; Condensation;90%
With triethylamine In tert-butyl alcohol at 35℃; industrial alkaline protease alcalase, 3 to 4 h;86%
4-(3-fluoro-benzyloxy)-benzaldehyde
66742-57-2

4-(3-fluoro-benzyloxy)-benzaldehyde

(S)-alaninamide hydrochloride
33208-99-0

(S)-alaninamide hydrochloride

safinamide
133865-89-1

safinamide

Conditions
ConditionsYield
Stage #1: (S)-alaninamide hydrochloride With triethylamine In methanol at 30℃; for 0.166667h;
Stage #2: 4-(3-fluoro-benzyloxy)-benzaldehyde In methanol at 20℃; for 3.5h;
Stage #3: With sodium tetrahydroborate In methanol at 5℃; for 2h; Product distribution / selectivity;		90%
Stage #1: 4-(3-fluoro-benzyloxy)-benzaldehyde; (S)-alaninamide hydrochloride With triethylamine In methanol at 20 - 25℃; for 1h;
Stage #2: With hydrogen; 5 % platinum on carbon In methanol at 20 - 35℃; under 750.075 - 3750.38 Torr; for 5h; Product distribution / selectivity;		90%
Stage #1: (S)-alaninamide hydrochloride With triethylamine In methanol at 30℃; for 0.166667h;
Stage #2: 4-(3-fluoro-benzyloxy)-benzaldehyde In methanol at 30℃; for 3.5h;
Stage #3: With sodium hydroxide; sodium tetrahydroborate In methanol; water at 5℃; for 2h; Product distribution / selectivity;		88.5%
4-((2-fluorobenzyl)oxy)benzaldehyde
70627-20-2

4-((2-fluorobenzyl)oxy)benzaldehyde

(S)-alaninamide hydrochloride
33208-99-0

(S)-alaninamide hydrochloride

(S)-2-[4-(2-fluorobenzyloxy)benzylideneamino]propanamide
1000370-32-0

(S)-2-[4-(2-fluorobenzyloxy)benzylideneamino]propanamide

Conditions
ConditionsYield
With triethylamine In methanol at 20℃; for 1h;90%
3-((2,3-dihydrobenzo[b][1,4]dioxin-5-oxy)methyl)benzaldehyde

3-((2,3-dihydrobenzo[b][1,4]dioxin-5-oxy)methyl)benzaldehyde

(S)-alaninamide hydrochloride
33208-99-0

(S)-alaninamide hydrochloride

(S)-2-(3-((2,3-dihydrobenzo[b][1,4]dioxin-5-oxy)methyl)benzylamino)propionamide

(S)-2-(3-((2,3-dihydrobenzo[b][1,4]dioxin-5-oxy)methyl)benzylamino)propionamide

Conditions
ConditionsYield
Stage #1: (S)-alaninamide hydrochloride With triethylamine In methanol at 20℃; for 0.5h;
Stage #2: 3-((2,3-dihydrobenzo[b][1,4]dioxin-5-oxy)methyl)benzaldehyde In methanol at 20℃; for 2h;
Stage #3: With potassium borohydride In methanol for 3h; Reflux;		88.83%
3-((2,3-dihydrobenzo[b]thiophen-7-oxy)methyl)benzaldehyde

3-((2,3-dihydrobenzo[b]thiophen-7-oxy)methyl)benzaldehyde

(S)-alaninamide hydrochloride
33208-99-0

(S)-alaninamide hydrochloride

(S)-2-(3-((2,3-dihydrobenzo[b]thiophen-7-oxy)methyl)benzylamino)propanamide

(S)-2-(3-((2,3-dihydrobenzo[b]thiophen-7-oxy)methyl)benzylamino)propanamide

Conditions
ConditionsYield
Stage #1: (S)-alaninamide hydrochloride With triethylamine In methanol at 20℃; for 0.5h;
Stage #2: 3-((2,3-dihydrobenzo[b]thiophen-7-oxy)methyl)benzaldehyde In methanol at 20℃; for 2h;
Stage #3: With potassium borohydride In methanol for 3h; Reflux;		88.65%
4-((2,3-dihydrobenzofuran-5-oxy)methyl)benzaldehyde

4-((2,3-dihydrobenzofuran-5-oxy)methyl)benzaldehyde

(S)-alaninamide hydrochloride
33208-99-0

(S)-alaninamide hydrochloride

(S)-2-(4-((2,3-dihydrobenzofuran-5-oxy)methyl)benzylamino)propanamide

(S)-2-(4-((2,3-dihydrobenzofuran-5-oxy)methyl)benzylamino)propanamide

Conditions
ConditionsYield
Stage #1: (S)-alaninamide hydrochloride With triethylamine In methanol at 20℃; for 0.5h;
Stage #2: 4-((2,3-dihydrobenzofuran-5-oxy)methyl)benzaldehyde In methanol at 20℃; for 2h;
Stage #3: With potassium borohydride In methanol for 3h; Reflux;		88.31%
4-((1H-benzo[d]imidazole-4-oxy)methyl)benzaldehyde

4-((1H-benzo[d]imidazole-4-oxy)methyl)benzaldehyde

(S)-alaninamide hydrochloride
33208-99-0

(S)-alaninamide hydrochloride

(S)-2-((4-(((1H-benzo[d]imidazol-4-yl)oxy)methyl)benzyl)amino)propanamide

(S)-2-((4-(((1H-benzo[d]imidazol-4-yl)oxy)methyl)benzyl)amino)propanamide

Conditions
ConditionsYield
Stage #1: (S)-alaninamide hydrochloride With triethylamine In methanol at 20℃; for 0.5h;
Stage #2: 4-((1H-benzo[d]imidazole-4-oxy)methyl)benzaldehyde In methanol at 20℃; for 2h;
Stage #3: With potassium borohydride In methanol for 3h; Reflux;		88.06%
Stage #1: (S)-alaninamide hydrochloride With triethylamine In methanol at 20℃; for 1h;
Stage #2: 4-((1H-benzo[d]imidazole-4-oxy)methyl)benzaldehyde In methanol for 2h;
Stage #3: With potassium borohydride In methanol for 3h; Reflux;		88%
(S)-alaninamide hydrochloride
33208-99-0

(S)-alaninamide hydrochloride

N-(benzyloxycarbonyl)-L-phenylalanine benzyl ester
60379-01-3

N-(benzyloxycarbonyl)-L-phenylalanine benzyl ester

N-(benzyloxycarbonyl)phenylalanyl-alanine amide
65118-54-9

N-(benzyloxycarbonyl)phenylalanyl-alanine amide

Conditions
ConditionsYield
With S166C-SCH2CH2NH3+; triethylamine; calcium chloride In water; N,N-dimethyl-formamide Ambient temperature;88%
With triethylamine; wild-type serine protease subtilisin Bacillus lentus In water; N,N-dimethyl-formamide at 20℃; for 24h; pH=5.8;57%
benzyl-(S)-(-)-2-hydroxy-3-phenylpropionate
7622-21-1

benzyl-(S)-(-)-2-hydroxy-3-phenylpropionate

(S)-alaninamide hydrochloride
33208-99-0

(S)-alaninamide hydrochloride

(S)-N-((S)-1-Carbamoyl-ethyl)-2-hydroxy-3-phenyl-propionamide

(S)-N-((S)-1-Carbamoyl-ethyl)-2-hydroxy-3-phenyl-propionamide

Conditions
ConditionsYield
With subtilisin bacillus lentus S166C-S-CH2C6F5 mutant enzyme; triethylamine In water; N,N-dimethyl-formamide at 20℃; for 48h;88%

L-Alaninamide hydrochloride Chemical Properties

IUPAC Name:(2S)-2-aminopropanamide hydrochloride
Molecular Formula:C3H9ClN2O
Molecular Weight:124.569360 g/mol
Appearance:white to light yellow crystal powder
Melting Point:212-217 °C
alpha:11 °(c=1, MeOH)
storage temp.:2-8 °C
Synonyms of L-Alaninamide hydrochloride(33208-99-0):
(S)-2-AMINOPROPIONAMIDE HYDROCHLORIDE;L-ALANAMINE HCL;(L)-ALANINAMIDE HCL;L-ALANINAMIDE HYDROCHLORIDE;L-ALANINE AMIDE HYDROCHLORIDE;H-L-ALA-NH2 HCL;H-ALA-NH2 HCL;H-ALA-NH2 HYDROCHLORIDE
Categories of L-Alaninamide hydrochloride(33208-99-0):
chiral;Amino Acids;Alanine [Ala, A];Amino hydrochloride;Alanine;Amino Acid Derivatives;Peptide Synthesis

L-Alaninamide hydrochloride Uses

L-Alaninamide hydrochloride(33208-99-0) is used for biochemical research.

L-Alaninamide hydrochloride Safety Profile

Safety Information of L-Alaninamide hydrochloride(33208-99-0):
Hazard Codes:C

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