Fmoc-L-homophenylalanine supplier

Name
Fmoc-L-homophenylalanine
EINECS
CAS No. 132684-59-4
Article Data2
CAS DataBase
Density 1.255 g/cm³
Solubility Slightly soluble in water.
Melting Point 141.0 to 145.0 °C
Formula C₂₅H₂₃NO₄
Boiling Point 628.284 °C at 760 mmHg
Molecular Weight 401.462
Flash Point 333.774 °C
Transport Information
Appearance
Safety 22-24/25
Risk Codes 36/37/38
Molecular Structure
Hazard Symbols Xi
Synonyms Benzenebutanoicacid, a-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-,(S)-;(S)-N-Fmoc-homophenylalanine;NPC 14686;
PSA 75.63000
LogP 5.00200

Synthetic route

: 943-73-7
D-homophenylalanine

: 82911-69-1
N-(9H-fluoren-2-ylmethoxycarbonyloxy)succinimide

: 132684-59-4
N-(fluorenyl-9-methoxycarbonyl)-L-homophenylalanine

Conditions

Conditions	Yield
With sodium carbonate In 1,4-dioxane; water at 20℃; for 18h;

: 14533-84-7
pentafluorophenyl trifloroacetate

: 132684-59-4
N-(fluorenyl-9-methoxycarbonyl)-L-homophenylalanine

: 839719-69-6
pentafluorophenyl L-α-[(9H-fluoren-9-ylmethoxycarbonyl)amino]benzenebutanoate

Conditions

Conditions	Yield
With pyridine In N,N-dimethyl-formamide at 20℃; for 1h;	96%

: (S)-2-cyclohexyl-2-(3,4,5-trimethoxyphenyl)acetic acid

: 101555-63-9, 105751-19-7, 86069-86-5
(S)-1-(((9H-fluoren-9-yl)methoxy)carbonyl)piperidine-2-carboxylic acid

: 132684-59-4
N-(fluorenyl-9-methoxycarbonyl)-L-homophenylalanine

: (S)-N-((S)-1-amino-1-oxo-4-phenylbutan-2-yl)-1-((S)-2-cyclohexyl-2-(3,4,5-trimethoxyphenyl)acetyl)piperidine-2-carboxamide

Conditions

Conditions	Yield
Stage #1: N-(fluorenyl-9-methoxycarbonyl)-L-homophenylalanine With benzotriazol-1-ol; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; for 2h; Stage #2: With 4-methylpiperidin In N,N-dimethyl-formamide at 20℃; for 0.333333h; Sieber amide resin; Stage #3: (S)-2-cyclohexyl-2-(3,4,5-trimethoxyphenyl)acetic acid; (S)-1-(((9H-fluoren-9-yl)methoxy)carbonyl)piperidine-2-carboxylic acid Further stages;	72.5%

Yield

Stage #1: N-(fluorenyl-9-methoxycarbonyl)-L-homophenylalanine With benzotriazol-1-ol; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; for 2h;
Stage #2: With 4-methylpiperidin In N,N-dimethyl-formamide at 20℃; for 0.333333h; Sieber amide resin;
Stage #3: (S)-2-cyclohexyl-2-(3,4,5-trimethoxyphenyl)acetic acid; (S)-1-(((9H-fluoren-9-yl)methoxy)carbonyl)piperidine-2-carboxylic acid Further stages;

72.5%

...Expand

: 35661-40-6
N-Fmoc L-Phe

: 132684-59-4
N-(fluorenyl-9-methoxycarbonyl)-L-homophenylalanine

: C19H23N3O2

Conditions

Conditions	Yield
Stage #1: N-(fluorenyl-9-methoxycarbonyl)-L-homophenylalanine With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In N,N-dimethyl-formamide Rink amide MBHA resin; Stage #2: With piperidine In N,N-dimethyl-formamide Rink amide MBHA resin; Stage #3: N-Fmoc L-Phe Further stages;	67%

: N'-[(9H-fluoren-9-ylmethoxy)carbonyl]-1H-imidazole-1-carbohydrazide

: (S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(3-fluorophenyl)propanoic acid

: 115951-16-1
1-tert-butoxycarbonylaminocyclohexanecarboxylic acid

: 132684-59-4
N-(fluorenyl-9-methoxycarbonyl)-L-homophenylalanine

: 1-(1-aminocyclohexane-1-carbonyl)-4-[2S-N-[2S-3-(m-fluorophenyl)propan-2-yl-amide]-4-phenylbutan-2-yl-amide]semicarbazide

Conditions

Conditions	Yield
Multistep reaction;	60%

...Expand

: 35661-60-0
Fmoc-Leu-OH

: 71989-31-6
Fmoc-Pro-OH

: 71989-16-7
Fmoc-Asn-OH

: 91000-69-0
Fmoc-L-Arg-OH

: 132684-59-4
N-(fluorenyl-9-methoxycarbonyl)-L-homophenylalanine

: 76-05-1
trifluoroacetic acid

: 501-52-0
3-Phenylpropionic acid

: C46H70N14O8*C2HF3O2

Conditions

Conditions	Yield
Stage #1: Fmoc-Asn-OH With benzotriazol-1-ol; diisopropyl-carbodiimide In N,N-dimethyl-formamide for 2h; Stage #2: With piperidine In N,N-dimethyl-formamide for 0.333333h; Stage #3: Fmoc-Leu-OH; Fmoc-Pro-OH; Fmoc-L-Arg-OH; N-(fluorenyl-9-methoxycarbonyl)-L-homophenylalanine; trifluoroacetic acid; 3-Phenylpropionic acid Further stages;	60%

...Expand

: N'-[(9H-fluoren-9-ylmethoxy)carbonyl]-1H-imidazole-1-carbohydrazide

: (S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(3-fluorophenyl)propanoic acid

: 132684-59-4
N-(fluorenyl-9-methoxycarbonyl)-L-homophenylalanine

: 135112-27-5
(S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)butanoic acid

: 1-(2S-2-aminobutanoyl)-4-[2S-N-[2S-3-(m-fluorophenyl)propan-2-yl-amide]-4-phenylbutan-2-yl-amide]semicarbazide

Conditions

Conditions	Yield
Multistep reaction;	54%

...Expand

: N'-[(9H-fluoren-9-ylmethoxy)carbonyl]-1H-imidazole-1-carbohydrazide

: 71989-31-6
Fmoc-Pro-OH

: 35737-15-6
Fmoc-Trp-OH

: 132684-59-4
N-(fluorenyl-9-methoxycarbonyl)-L-homophenylalanine

: C27H33N7O4

Conditions

Conditions	Yield
Multistep reaction;	51%

...Expand

: 132684-59-4
N-(fluorenyl-9-methoxycarbonyl)-L-homophenylalanine

: 71989-33-8, 128107-47-1
Nα-(9-fluorenylmethoxycarbonyl)-D-serine-tert-butyl ether

: Nα-(9-fluorenylmethyloxycarbonyl)-Nγ-2,2,4,6,7-pentamethyldihydrobenzofuran-5-sulfonyl-L-arginine

: 1428768-33-5
C19H30N6O5

Conditions

Conditions	Yield
Stage #1: Nα-(9-fluorenylmethyloxycarbonyl)-Nγ-2,2,4,6,7-pentamethyldihydrobenzofuran-5-sulfonyl-L-arginine With benzotriazol-1-ol; diisopropyl-carbodiimide In 1-methyl-pyrrolidin-2-one; dichloromethane; N,N-dimethyl-formamide 2-chlorotrityl chloride resin; Stage #2: With piperidine In 1-methyl-pyrrolidin-2-one; N,N-dimethyl-formamide for 0.25h; 2-chlorotrityl chloride resin; Stage #3: N-(fluorenyl-9-methoxycarbonyl)-L-homophenylalanine; Nα-(9-fluorenylmethoxycarbonyl)-D-serine-tert-butyl ether Further stages;	51%

Yield

Stage #1: Nα-(9-fluorenylmethyloxycarbonyl)-Nγ-2,2,4,6,7-pentamethyldihydrobenzofuran-5-sulfonyl-L-arginine With benzotriazol-1-ol; diisopropyl-carbodiimide In 1-methyl-pyrrolidin-2-one; dichloromethane; N,N-dimethyl-formamide 2-chlorotrityl chloride resin;
Stage #2: With piperidine In 1-methyl-pyrrolidin-2-one; N,N-dimethyl-formamide for 0.25h; 2-chlorotrityl chloride resin;
Stage #3: N-(fluorenyl-9-methoxycarbonyl)-L-homophenylalanine; Nα-(9-fluorenylmethoxycarbonyl)-D-serine-tert-butyl ether Further stages;

51%

...Expand

: N'-[(9H-fluoren-9-ylmethoxy)carbonyl]-1H-imidazole-1-carbohydrazide

: 132684-59-4
N-(fluorenyl-9-methoxycarbonyl)-L-homophenylalanine

: 135112-27-5
(S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)butanoic acid

: (S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(3-methoxyphenyl)propanoic acid

: 1-(2S-2-aminobutanoyl)-4-[2S-N-[2S-3-(m-methoxyphenyl)propan-2-yl-amide]-4-phenylbutan-2-yl-amide]semicarbazide

Conditions

Conditions	Yield
Multistep reaction;	46%

...Expand

: N'-[(9H-fluoren-9-ylmethoxy)carbonyl]-1H-imidazole-1-carbohydrazide

: 35737-15-6
Fmoc-Trp-OH

: 132684-59-4
N-(fluorenyl-9-methoxycarbonyl)-L-homophenylalanine

: 135112-27-5
(S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)butanoic acid

: 1-(2S-2-aminobutanoyl)-4-[2S-N-[2S-3-(indol-3-yl)propan-2-yl-amide]-4-phenylbutan-2-2-yl-amide]semicarbazide

Conditions

Conditions	Yield
Multistep reaction;	28%

...Expand

: 35661-60-0
Fmoc-Leu-OH

: 71989-14-5
Fmoc-(tBu)Asp-OH

: 71989-18-9
Fmoc-Glu(OtBu)-OH

: 132684-59-4
N-(fluorenyl-9-methoxycarbonyl)-L-homophenylalanine

Fmoc-Gly: Fmoc-Gly

: c[L-homoPhe-L-homoPhe-L-Asp-L-Glu-Gly-L-Leu-L-Glu-L-Glu]-NH2

Conditions

Conditions	Yield
Multistep reaction.;	17%

...Expand

: N'-[(9H-fluoren-9-ylmethoxy)carbonyl]-1H-imidazole-1-carbohydrazide

: 132684-59-4
N-(fluorenyl-9-methoxycarbonyl)-L-homophenylalanine

: 135112-27-5
(S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)butanoic acid

: Fmoc-β-(3-benzothienyl)-L-alanine

: 1-(2S-2-aminobutanoyl)-4-[2S-N-[2S-3-(benzo[b]thiophen-3-yl)propan-2-yl-amide]-4-phenylbutan-2-yl-amide]semicarbazide

Conditions

Conditions	Yield
Multistep reaction;	16%

...Expand

: N'-[(9H-fluoren-9-ylmethoxy)carbonyl]-1H-imidazole-1-carbohydrazide

: 132684-59-4
N-(fluorenyl-9-methoxycarbonyl)-L-homophenylalanine

: 135112-27-5
(S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)butanoic acid

: N-[(9-fluorenyl)methoxycarbonyl]-4-chloro-L-phenylalanine

: 1-(2S-2-aminobutanoyl)-4-[2S-N-[2S-3-(p-chlorophenyl)propan-2-yl-amide]-4-phenylbutan-2-yl-amide]semicarbazide

Conditions

Conditions	Yield
Multistep reaction;	15%

...Expand

: 943-73-7
D-homophenylalanine

: 82911-69-1
N-(9H-fluoren-2-ylmethoxycarbonyloxy)succinimide

: 132684-59-4
N-(fluorenyl-9-methoxycarbonyl)-L-homophenylalanine

Conditions

Conditions	Yield
With sodium carbonate In 1,4-dioxane; water at 20℃; for 18h;

: 14533-84-7
pentafluorophenyl trifloroacetate

: 132684-59-4
N-(fluorenyl-9-methoxycarbonyl)-L-homophenylalanine

: 839719-69-6
pentafluorophenyl L-α-[(9H-fluoren-9-ylmethoxycarbonyl)amino]benzenebutanoate

Conditions

Conditions	Yield
With pyridine In N,N-dimethyl-formamide at 20℃; for 1h;	96%

: (S)-2-cyclohexyl-2-(3,4,5-trimethoxyphenyl)acetic acid

: 101555-63-9, 105751-19-7, 86069-86-5
(S)-1-(((9H-fluoren-9-yl)methoxy)carbonyl)piperidine-2-carboxylic acid

: 132684-59-4
N-(fluorenyl-9-methoxycarbonyl)-L-homophenylalanine

: (S)-N-((S)-1-amino-1-oxo-4-phenylbutan-2-yl)-1-((S)-2-cyclohexyl-2-(3,4,5-trimethoxyphenyl)acetyl)piperidine-2-carboxamide

Conditions

Conditions	Yield
Stage #1: N-(fluorenyl-9-methoxycarbonyl)-L-homophenylalanine With benzotriazol-1-ol; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; for 2h; Stage #2: With 4-methylpiperidin In N,N-dimethyl-formamide at 20℃; for 0.333333h; Sieber amide resin; Stage #3: (S)-2-cyclohexyl-2-(3,4,5-trimethoxyphenyl)acetic acid; (S)-1-(((9H-fluoren-9-yl)methoxy)carbonyl)piperidine-2-carboxylic acid Further stages;	72.5%

Yield

72.5%

...Expand

: 35661-40-6
N-Fmoc L-Phe

: 132684-59-4
N-(fluorenyl-9-methoxycarbonyl)-L-homophenylalanine

: C19H23N3O2

Conditions

Conditions	Yield
Stage #1: N-(fluorenyl-9-methoxycarbonyl)-L-homophenylalanine With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In N,N-dimethyl-formamide Rink amide MBHA resin; Stage #2: With piperidine In N,N-dimethyl-formamide Rink amide MBHA resin; Stage #3: N-Fmoc L-Phe Further stages;	67%

: N'-[(9H-fluoren-9-ylmethoxy)carbonyl]-1H-imidazole-1-carbohydrazide

: (S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(3-fluorophenyl)propanoic acid

: 115951-16-1
1-tert-butoxycarbonylaminocyclohexanecarboxylic acid

: 132684-59-4
N-(fluorenyl-9-methoxycarbonyl)-L-homophenylalanine

: 1-(1-aminocyclohexane-1-carbonyl)-4-[2S-N-[2S-3-(m-fluorophenyl)propan-2-yl-amide]-4-phenylbutan-2-yl-amide]semicarbazide

Conditions

Conditions	Yield
Multistep reaction;	60%

...Expand

: 35661-60-0
Fmoc-Leu-OH

: 71989-31-6
Fmoc-Pro-OH

: 71989-16-7
Fmoc-Asn-OH

: 91000-69-0
Fmoc-L-Arg-OH

: 132684-59-4
N-(fluorenyl-9-methoxycarbonyl)-L-homophenylalanine

: 76-05-1
trifluoroacetic acid

: 501-52-0
3-Phenylpropionic acid

: C46H70N14O8*C2HF3O2

Conditions

Conditions	Yield
Stage #1: Fmoc-Asn-OH With benzotriazol-1-ol; diisopropyl-carbodiimide In N,N-dimethyl-formamide for 2h; Stage #2: With piperidine In N,N-dimethyl-formamide for 0.333333h; Stage #3: Fmoc-Leu-OH; Fmoc-Pro-OH; Fmoc-L-Arg-OH; N-(fluorenyl-9-methoxycarbonyl)-L-homophenylalanine; trifluoroacetic acid; 3-Phenylpropionic acid Further stages;	60%

...Expand

: N'-[(9H-fluoren-9-ylmethoxy)carbonyl]-1H-imidazole-1-carbohydrazide

: (S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(3-fluorophenyl)propanoic acid

: 132684-59-4
N-(fluorenyl-9-methoxycarbonyl)-L-homophenylalanine

: 135112-27-5
(S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)butanoic acid

: 1-(2S-2-aminobutanoyl)-4-[2S-N-[2S-3-(m-fluorophenyl)propan-2-yl-amide]-4-phenylbutan-2-yl-amide]semicarbazide

Conditions

Conditions	Yield
Multistep reaction;	54%

...Expand

: N'-[(9H-fluoren-9-ylmethoxy)carbonyl]-1H-imidazole-1-carbohydrazide

: 71989-31-6
Fmoc-Pro-OH

: 35737-15-6
Fmoc-Trp-OH

: 132684-59-4
N-(fluorenyl-9-methoxycarbonyl)-L-homophenylalanine

: C27H33N7O4

Conditions

Conditions	Yield
Multistep reaction;	51%

...Expand

: 132684-59-4
N-(fluorenyl-9-methoxycarbonyl)-L-homophenylalanine

: 71989-33-8, 128107-47-1
Nα-(9-fluorenylmethoxycarbonyl)-D-serine-tert-butyl ether

: Nα-(9-fluorenylmethyloxycarbonyl)-Nγ-2,2,4,6,7-pentamethyldihydrobenzofuran-5-sulfonyl-L-arginine

: 1428768-33-5
C19H30N6O5

Conditions

Conditions	Yield
Stage #1: Nα-(9-fluorenylmethyloxycarbonyl)-Nγ-2,2,4,6,7-pentamethyldihydrobenzofuran-5-sulfonyl-L-arginine With benzotriazol-1-ol; diisopropyl-carbodiimide In 1-methyl-pyrrolidin-2-one; dichloromethane; N,N-dimethyl-formamide 2-chlorotrityl chloride resin; Stage #2: With piperidine In 1-methyl-pyrrolidin-2-one; N,N-dimethyl-formamide for 0.25h; 2-chlorotrityl chloride resin; Stage #3: N-(fluorenyl-9-methoxycarbonyl)-L-homophenylalanine; Nα-(9-fluorenylmethoxycarbonyl)-D-serine-tert-butyl ether Further stages;	51%

Yield

51%

...Expand

: N'-[(9H-fluoren-9-ylmethoxy)carbonyl]-1H-imidazole-1-carbohydrazide

: 132684-59-4
N-(fluorenyl-9-methoxycarbonyl)-L-homophenylalanine

: 135112-27-5
(S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)butanoic acid

: (S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(3-methoxyphenyl)propanoic acid

: 1-(2S-2-aminobutanoyl)-4-[2S-N-[2S-3-(m-methoxyphenyl)propan-2-yl-amide]-4-phenylbutan-2-yl-amide]semicarbazide

Conditions

Conditions	Yield
Multistep reaction;	46%

...Expand

: N'-[(9H-fluoren-9-ylmethoxy)carbonyl]-1H-imidazole-1-carbohydrazide

: 35737-15-6
Fmoc-Trp-OH

: 132684-59-4
N-(fluorenyl-9-methoxycarbonyl)-L-homophenylalanine

: 135112-27-5
(S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)butanoic acid

: 1-(2S-2-aminobutanoyl)-4-[2S-N-[2S-3-(indol-3-yl)propan-2-yl-amide]-4-phenylbutan-2-2-yl-amide]semicarbazide

Conditions

Conditions	Yield
Multistep reaction;	28%

...Expand

: 35661-60-0
Fmoc-Leu-OH

: 71989-14-5
Fmoc-(tBu)Asp-OH

: 71989-18-9
Fmoc-Glu(OtBu)-OH

: 132684-59-4
N-(fluorenyl-9-methoxycarbonyl)-L-homophenylalanine

Fmoc-Gly: Fmoc-Gly

: c[L-homoPhe-L-homoPhe-L-Asp-L-Glu-Gly-L-Leu-L-Glu-L-Glu]-NH2

Conditions

Conditions	Yield
Multistep reaction.;	17%

...Expand

: N'-[(9H-fluoren-9-ylmethoxy)carbonyl]-1H-imidazole-1-carbohydrazide

: 132684-59-4
N-(fluorenyl-9-methoxycarbonyl)-L-homophenylalanine

: 135112-27-5
(S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)butanoic acid

: Fmoc-β-(3-benzothienyl)-L-alanine

: 1-(2S-2-aminobutanoyl)-4-[2S-N-[2S-3-(benzo[b]thiophen-3-yl)propan-2-yl-amide]-4-phenylbutan-2-yl-amide]semicarbazide

Conditions

Conditions	Yield
Multistep reaction;	16%

...Expand

: N'-[(9H-fluoren-9-ylmethoxy)carbonyl]-1H-imidazole-1-carbohydrazide

: 132684-59-4
N-(fluorenyl-9-methoxycarbonyl)-L-homophenylalanine

: 135112-27-5
(S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)butanoic acid

: N-[(9-fluorenyl)methoxycarbonyl]-4-chloro-L-phenylalanine

: 1-(2S-2-aminobutanoyl)-4-[2S-N-[2S-3-(p-chlorophenyl)propan-2-yl-amide]-4-phenylbutan-2-yl-amide]semicarbazide

Conditions

Conditions	Yield
Multistep reaction;	15%

...Expand

Fmoc-L-homophenylalanine Specification

The IUPAC name of Fmoc-L-Homo-phe-OH is (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-4-phenylbutanoic acid. With the CAS registry number 132684-59-4, it is also named as (S)-N-Fmoc-homophenylalanine. The product's categories are Phenylalanine Analogs and other Aromatic Alpha Amino Acids; Amino Acids; Unusual Amino Acids. In addition, its molecular formula is C₂₅H₂₃NO₄ and its molecular weight is 401.45. This chemical is white powder which should be sealed at 2-8 °C. Besides, when you are using this chemical, please do not breathe dust. And you should avoid contact with skin and eyes.

The other characteristics of Fmoc-L-Homo-phe-OH can be summarized as: (1)ACD/LogP: 5.89; (2)# of Rule of 5 Violations: 1; (3)ACD/LogD (pH 5.5): 3.82; (4)ACD/LogD (pH 7.4): 2.34; (5)ACD/BCF (pH 5.5): 149.62; (6)ACD/BCF (pH 7.4): 4.97; (7)ACD/KOC (pH 5.5): 324.11; (8)ACD/KOC (pH 7.4): 10.77; (9)#H bond acceptors: 5; (10)#H bond donors: 2; (11)#Freely Rotating Bonds: 8; (12)Polar Surface Area: 55.84 Å²; (13)Index of Refraction: 1.624; (14)Molar Refractivity: 113.03 cm³; (15)Molar Volume: 319.9 cm³; (16)Polarizability: 44.81×10^-24cm³; (17)Surface Tension: 55.7 dyne/cm; (18)Density: 1.254 g/cm³; (19)Flash Point: 333.8 °C; (20)Enthalpy of Vaporization: 97.72 kJ/mol; (21)Boiling Point: 628.3 °C at 760 mmHg; (22)Vapour Pressure: 1.19E-16 mmHg at 25 °C.

People can use the following data to convert to the molecule structure.
(1)SMILES: O=C(O)[C@@H](NC(=O)OCC3c1ccccc1c2c3cccc2)CCc4ccccc4
(2)InChI: InChI=1/C25H23NO4/c27-24(28)23(15-14-17-8-2-1-3-9-17)26-25(29)30-16-22-20-12-6-4-10-18(20)19-11-5-7-13-21(19)22/h1-13,22-23H,14-16H2,(H,26,29)(H,27,28)/t23-/m0/s1
(3)InChIKey: CIHPCIUGLIZADU-QHCPKHFHBA
(4)Std. InChI: InChI=1S/C25H23NO4/c27-24(28)23(15-14-17-8-2-1-3-9-17)26-25(29)30-16-22-20-12-6-4-10-18(20)19-11-5-7-13-21(19)22/h1-13,22-23H,14-16H2,(H,26,29)(H,27,28)/t23-/m0/s1
(5)Std. InChIKey: CIHPCIUGLIZADU-QHCPKHFHSA-N

Product Name

Fmoc-L-homophenylalanine

Synthetic route

Fmoc-L-homophenylalanine Specification

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