CAS Number67336-19-0
Synonymsp-chloroanilinoacetic acid; DL-p-chlorophenylglycine; (4-Chloro-phenylamino)-acetic acid; F3308-1184; N-(4-chlorophenyl)-glycine; (p-chlorophenyl)-glycine; (4-chlorophenyl)glycine; [(4-Chlorophenyl)amino]acetic acid; n-(4-chlorphenyl)glycin; 2-((4-chlorophenyl)amino)acetic acid; N-(4-Chlorophenyl)glycine; MFCD03701467; (s)-amino-(4-chloro-phenyl)-acetic acid; Amino(4-chlorophenyl)acetic acid; H-Phg(4-Cl)-OH
Molecular FormulaC8H8ClNO2
Molecular Weight185.61
Purity98.00%
Density1.4±0.1 g/cm3
Boiling Point412.5±25.0 °C at 760 mmHg
Melting Point266 °C(dec.)
AppearanceSolid;White to Almost white powder to crystal
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 67336-19-0 |
| Catalog No. | 2A-9046550 |
| Chinese Name | (S)-4-氯苯甘氨酸 |
| Synonyms | p-chloroanilinoacetic acid; DL-p-chlorophenylglycine; (4-Chloro-phenylamino)-acetic acid; F3308-1184; N-(4-chlorophenyl)-glycine; (p-chlorophenyl)-glycine; (4-chlorophenyl)glycine; [(4-Chlorophenyl)amino]acetic acid; n-(4-chlorphenyl)glycin; 2-((4-chlorophenyl)amino)acetic acid; N-(4-Chlorophenyl)glycine; MFCD03701467; (s)-amino-(4-chloro-phenyl)-acetic acid; Amino(4-chlorophenyl)acetic acid; H-Phg(4-Cl)-OH |
| Molecular Formula | C8H8ClNO2 |
| Molecular Weight | 185.61 |
| Purity | 98.00 |
| Density | 1.4±0.1 g/cm3 |
| Boiling Point | 412.5±25.0 °C at 760 mmHg |
| Melting Point | 266 °C(dec.) |
| Appearance | Solid;White to Almost white powder to crystal |
| Storage Condition | room temperature, dry |
| Application | H-Phg(4-Cl)-OH is a derivative of glycine (HY-Y0966) [1]. |
| HTC | 2922499990 |
| PubChem ID | 9312136 |
| SMILES | NC(C(=O)O)c1ccc(Cl)cc1 |
| InChI | InChI=1S/C8H8ClNO2/c9-6-3-1-5(2-4-6)7(10)8(11)12/h1-4,7H,10H2,(H,11,12)/t7-/m0/s1 |
| InChI Key | QGJGBYXRJVIYGA-ZETCQYMHSA-N |
| Use of | H-Phg(4-Cl)-OH is a Glycine (HY-Y0966) derivative[1]. Properties Name (S)-2-Amino-2-(4-chlorophenyl)acetic acid Synonym More Synonyms H-Phg(4-Cl)-OH Biological Activity Description H-Phg(4-Cl)-OH is a Glycine (HY-Y0966) derivative[1]. Related Catalog Research Areas >> Others Signaling Pathways >> Others >> Others In Vitro Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1]. References [1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144. Chemical & Physical Properties Exact Mass 185.024353 PSA 63.32000 Index of Refraction 1.630 InChIKey QGJGBYXRJVIYGA-ZETCQYMHSA-N Safety Information Hazard Codes T Risk Phrases 25 Safety Phrases 45 HS Code 2922499990 Precursor & DownStream Precursor 5 CAS#:86169-29-1 (2S)-2-acetamid... CAS#:104-88-1 4-Chlorobenzaldehyde CAS#:856214-68-1 4-chloro-N-(2,3... CAS#:102333-75-5 2-amino-2-(4-ch... DownStream 0 |
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