Detail of > 13921-90-9
- CAS Number:
- 13921-90-9
- Name:
Benzenepropanoic acid, b-amino-, (bR)-
- Superlist Name:
- (R)-3-Amino-3-phenylpropionic acid
- Formula:
- C9H11NO2
- Molecular Structure:

- Synonyms:
- Benzenepropanoicacid, b-amino-, (R)-;Hydrocinnamicacid, b-amino-, L- (8CI);(+)-3-Amino-3-phenylpropanoic acid;(R)-3-Amino-3-phenylpropanoic acid;(R)-b-Phenylalanine;L-3-Amino-3-phenylpropionic acid;L-b-Phenyl-b-alanine;
- Molecular Weight:
- 165.19
- Density:
- 1.199 g/cm3
- Boiling Point:
- 307.522 °C at 760 mmHg
- Flash Point:
- 139.785 °C
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Reference
- Enzymatic method for the enantiomeric resolution of amino acids
- Enzymatic method for the enantiomeric resolution of amino acids. Salagnad, Christophe; Gobert, Claude; Dury, Marie-odile (Aventis Pharma S.A., Fr.). PCT Int. Appl. WO 2003020943 A2 13 Mar 2003, 23 pp. DESIGNATED STATES: W: AE, AG, AL, AM, AT, AU, AZ, BA, BB, BG, BR, BY, BZ, CA, CH, CN, CO, CR, CU, CZ, DE, DK, DM, DZ, EC, EE, ES, FI, GB, GD, GE, GH, GM, HR, HU, ID, IL, IN, IS, JP, KE, KG, KP, KR, KZ, LC, LK, LR, LS, LT, LU, LV, MA, MD, MG, MK, MN, MW, MX, MZ, NO, NZ, OM, PH, PL, PT, RO, RU, SD, SE, SG, SI, SK, SL, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, YU, ZA, ZM, ZW, AM, AZ, BY, KG, KZ, MD, RU, TJ, TM; RW: AT, BE, BF, BJ, CF, CG, CH, CI, CM, CY, DE, DK, ES, FI, FR, GA, GB, GR, IE, IT, LU, MC, ML, MR, NE, NL, PT, SE, SN, TD, TG, TR. (French).Some commonly used reagents like 13921-90-9 is used in this experiment. (World Intellectual Property Organization). CODEN: PIXXD2. CLASS: ICM: C12P013-04. ICS: C12P041-00; C12N009-80. APPLICATION: WO 2002-FR2976 30 Aug 2002. PRIORITY: FR 2001-11431 4 Sep 2001; US 2001-PV331613 20 Nov 2001. DOCUMENT TYPE: Patent CA Section: 16 (Fermentation and Bioindustrial Chemistry) The invention relates to a novel enzymic method that is used for the enantiomeric resoln. of amino acids. More specifically, said method of sepg.There are some reagents like 13921-90-9 is used in this study. the enantiomers of an amino acid consists in treating a racemic mixt. of said amino acid with glutaric anhydride and subsequently with the glutaryl 7-aminocephalosporanic acid acylase enzyme such that one of the enantiomers of said amino acid is recovered, while the other enantiomer remains in the form of a deriv. of the corresponding glutaryl amide. ..
- Enzymatic method for the enantiomeric resolution of amino acids
- Enzymatic method for the enantiomeric resolution of amino acids. Salagnad, Christophe; Gobert, Claude; Dury, Marie-odile (Aventis Pharma S.A., Fr.). PCT Int. Appl. WO 2003020943 A2 13 Mar 2003, 23 pp. DESIGNATED STATES: W: AE, AG, AL, AM, AT, AU, AZ, BA, BB, BG, BR, BY, BZ, CA, CH, CN, CO, CR, CU, CZ, DE, DK, DM, DZ, EC, EE, ES, FI, GB, GD, GE, GH, GM, HR, HU, ID, IL, IN, IS, JP, KE, KG, KP, KR, KZ, LC, LK, LR, LS, LT, LU, LV, MA, MD, MG, MK, MN, MW, MX, MZ, NO, NZ, OM, PH, PL, PT, RO, RU, SD, SE, SG, SI, SK, SL, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, YU, ZA, ZM, ZW, AM, AZ, BY, KG, KZ, MD, RU, TJ, TM; RW: AT, BE, BF, BJ, CF, CG, CH, CI, CM, CY, DE, DK, ES, FI, FR, GA, GB, GR, IE, IT, LU, MC, ML, MR, NE, NL, PT, SE, SN, TD, TG, TR. (French).Some commonly used reagents like 13921-90-9 is used in this experiment. (World Intellectual Property Organization). CODEN: PIXXD2. CLASS: ICM: C12P013-04. ICS: C12P041-00; C12N009-80. APPLICATION: WO 2002-FR2976 30 Aug 2002. PRIORITY: FR 2001-11431 4 Sep 2001; US 2001-PV331613 20 Nov 2001. DOCUMENT TYPE: Patent CA Section: 16 (Fermentation and Bioindustrial Chemistry) The invention relates to a novel enzymic method that is used for the enantiomeric resoln. of amino acids. More specifically, said method of sepg.There are some reagents like 13921-90-9 is used in this study. the enantiomers of an amino acid consists in treating a racemic mixt. of said amino acid with glutaric anhydride and subsequently with the glutaryl 7-aminocephalosporanic acid acylase enzyme such that one of the enantiomers of said amino acid is recovered, while the other enantiomer remains in the form of a deriv. of the corresponding glutaryl amide. ..
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