Detail of > 710-11-2
- CAS Number:
- 710-11-2
- Name:
Benzenebutanoic acid, a-oxo-
- Superlist Name:
- 2-Oxo-4-phenylbutyric acid
- Formula:
- C10H10O3
- Molecular Structure:

- Synonyms:
- Butyricacid, 2-oxo-4-phenyl- (6CI,7CI,8CI);2-Oxo-4-phenylbutanoic acid;4-Phenyl-2-oxobutanoic acid;4-Phenyl-2-oxobutyricacid;Benzylpyruvic acid;
- Molecular Weight:
- 178.18
- EINECS:
- 211-916-7
- Density:
- 1.212 g/cm3
- Boiling Point:
- 314.4 °C at 760 mmHg
- Flash Point:
- 158.1 °C
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Reference
- N-Carboxymethyl-substituted lysyl and a-(e-aminoalkyl)glycyl amino acid antihypertensive agents
- N-Carboxymethyl-substituted lysyl and a-(e-aminoalkyl)glycyl amino acid antihypertensive agents. Patchett, Arthur A.; Wu, Mu T. (Merck and Co., Inc. , USA). S. African ZA 8302508 A 28 Nov 1984, 51 pp. (English). (South Rica). CODEN: SFXXAB. CLASS: ICM: A61K. ICS: C07C. APPLICATION: ZA 83-2508 11 Apr 1983. PRIORITY: US 82-367531 12 Apr 1982. DOCUMENT TYPE: Patent CA Section: 63 (Pharmaceuticals) Section cross-reference(s): 34 Novel N-carboxymethyl substituted lysyl and a-(e-aminoalkyl)glycyl amino acids, which are inhibitors of angiotensin I-converting enzymes, were formulated in pharmaceutical compns. and used to treat hypertension. 710-11-2 is the cas registry number of certain chemical which is used as reagents here. I was treated with 4-phenyl-2-oxobutanoic acid [710-11-2] to give N-[6-benzyloxycarbonylamino-2-(1-carboxy-3-phenylpropylamino)-5- hydroxyhexanoyl]-L-proline [96359-86-3], and the latter compd. was hydrogenated to give N-[6-amino-2-(1-carboxy-3-phenylpropylamino)-5-hydroxyhexanoyl-L -proline (II) [96359-87-4] which has antihypertensive activity. The synthesis of these amino acids was described. E.g. There are some commonly used reagents like 710-11-2 in this article., 5-hydroxy-L-lysine [1190-94-9] was converted to N-(2-amino-6-benzyloxycarbonylamino-5-hydroxyhexanoyl)-L-proline (I) [96359-85-2] by a series of blocking and deblocking reactions and reaction with L-proline tert-Bu ester [2812-46-6]. Compns. contg. the title compds. and known antihypertensives were described. ..
- N-Carboxymethyl-substituted lysyl and a-(e-aminoalkyl)glycyl amino acid antihypertensive agents
- N-Carboxymethyl-substituted lysyl and a-(e-aminoalkyl)glycyl amino acid antihypertensive agents. Patchett, Arthur A.; Wu, Mu T. (Merck and Co., Inc. , USA). S. African ZA 8302508 A 28 Nov 1984, 51 pp. (English). (South Rica). CODEN: SFXXAB. CLASS: ICM: A61K. ICS: C07C. APPLICATION: ZA 83-2508 11 Apr 1983. PRIORITY: US 82-367531 12 Apr 1982. DOCUMENT TYPE: Patent CA Section: 63 (Pharmaceuticals) Section cross-reference(s): 34 Novel N-carboxymethyl substituted lysyl and a-(e-aminoalkyl)glycyl amino acids, which are inhibitors of angiotensin I-converting enzymes, were formulated in pharmaceutical compns. and used to treat hypertension. 710-11-2 is the cas registry number of certain chemical which is used as reagents here. I was treated with 4-phenyl-2-oxobutanoic acid [710-11-2] to give N-[6-benzyloxycarbonylamino-2-(1-carboxy-3-phenylpropylamino)-5- hydroxyhexanoyl]-L-proline [96359-86-3], and the latter compd. was hydrogenated to give N-[6-amino-2-(1-carboxy-3-phenylpropylamino)-5-hydroxyhexanoyl-L -proline (II) [96359-87-4] which has antihypertensive activity. The synthesis of these amino acids was described. E.g. There are some commonly used reagents like 710-11-2 in this article., 5-hydroxy-L-lysine [1190-94-9] was converted to N-(2-amino-6-benzyloxycarbonylamino-5-hydroxyhexanoyl)-L-proline (I) [96359-85-2] by a series of blocking and deblocking reactions and reaction with L-proline tert-Bu ester [2812-46-6]. Compns. contg. the title compds. and known antihypertensives were described. ..
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