Detail of "17193-40-7"

CAS Number:
17193-40-7
Name:
L-4-Nitrophenylalanine methyl ester hydrochloride
Molecular Structure:
Formula:
C₁₀H₁₃ClN₂O₄
Molecular Weight:
260.67
Synonyms:
Alanine,3-(p-nitrophenyl)-, methyl ester, monohydrochloride, L- (8CI);L-Phenylalanine,4-nitro-, methyl ester, monohydrochloride (9CI);(S)-1-Methoxycarbonyl-2-(4-nitrophenyl)ethanaminium chloride;Methyl4-nitro-L-phenylalaninate hydrochloride;p-Nitrophenylalanine methyl esterhydrochloride;H-Phe(4-NO2)-OMe·OH;
Melting Point:
210-214 °C
Boiling Point:
360 °C at 760 mmHg
Flash Point:
171.5 °C
Risk Codes:
22
Safety:
22-36/37 Details
Transport Information:
UN 2811

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Reference

Method for preparing enantiomeric forms of amino alkylaminophenyl propanoic acid: Method for preparing enantiomeric forms of amino alkylaminophenyl propanoic acid. Stammler, Robert (Rhone-Poulenc Rorer S.A.; Stammler, Robert, Fr. 17193-40-7 and 57206-54-9 are also occured in this study.). PCT Int. Appl. WO 9641794 A1 27 Dec 1996, 20 pp. DESIGNATED STATES: W: AL, AU, BB, BG, BR, CA, CN, CZ, EE, GE, HU, IL, IS, JP, KP, KR, LK, LR, LT, LV, MG, MK, MN, MX, NO, NZ, PL, RO, SG, SI, SK, TR, TT, UA, US, UZ, VN, AM, AZ, BY, KG, KZ, MD, RU, TJ, TM; RW: AT, BE, BF, BJ, CF, CG, CH, CI, CM, DE, DK, ES, FI, FR, GA, GB, GR, IE, IT, LU, MC, ML, MR, NE, NL, PT, SE, SN, TD, TG. (French). (World Intellectual Property Organization). CODEN: PIXXD2. CLASS: ICM: C07C229-12. ICS: C07C227-14. APPLICATION: WO 1996-FR872 10 Jun 1996. PRIORITY: FR 1995-6890 12 Jun 1995. DOCUMENT TYPE: Patent CA Section: 34 (Amino Acids, Peptides, and Proteins) Title amino acids p-RNHC6H4CH2CH(NH2)CO2H (I; R = alkyl) were prepd. in (S) or (R) forms from L- or D-phenylalanine. Thus, L-phenylalanine underwent nitration, Me esterification, acetylation, nitro group redn., formylation-redn., and hydrolysis to afford (S)-I.2HCl (R = Me). The latter was used in the synthesis of pristinamycin IB. .

Synthesis of the Protein Cutting Reagent Iron (S)-1-(p-Bromoacetamidobenzyl)ethylenediaminetetraacetate and Conjugation to Cysteine Side Chains: Synthesis of the Protein Cutting Reagent Iron (S)-1-(p-Bromoacetamidobenzyl)ethylenediaminetetraacetate and Conjugation to Cysteine Side Chains. Greiner, Douglas P.; Miyake, Reiko; Moran, Justin K.; Jones, A. Daniel; Negishi, Tomofumi; Ishihama, Akira; Meares, Claude F. (Department of Chemistry, University of California, Davis, CA 95616, USA). Bioconjugate Chemistry, 8(1), 44-48 (English) 1997 American Chemical Society. CODEN: BCCHES. ISSN: 1043-1802. DOCUMENT TYPE: Journal CA Section: 9 (Biochemical Methods) Convenient methodol. for prepn. and conjugation of the protein-cutting iron chelate iron (S)-1-(p-bromoacetamidobenzyl)ethylenediaminetetraacetate (Fe-BABE) is given. This formulation of the reagent can be handled in a manner analogous to many other protein-labeling reagents, such as fluorescent probes or cross-linkers. By taking advantage of the recently discovered peptide hydrolysis reaction, the chelate may be tethered to a single site (e.g.There are some commonly used reagents with their cas registry numbers 79-08-3 and 17193-40-7 in this article., a cysteine side chain) and used to map its proximity to individual peptide bonds by automated Edman sequencing of the protein fragments produced. The method is illustrated by conjugation of Fe-BABE to the carboxy terminal domain (amino acid residues 234-329) of the Escherichia coli RNA polymerase alpha subunit. The mol. mass of the protein conjugate was confirmed by electrospray ionization mass spectrometry. .

Detail of "17193-40-7"

L-4-Nitrophenylalanine methyl ester hydrochloride

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CAS No.17193-40-7 L-4-Nitrophenylalanine methyl ester hydrochloride

CAS No.17193-40-7 L-4-Nitrophenylalanine methyl ester hydrochloride

CAS No.17193-40-7 L-4-Nitrophenylalanine methyl ester hydrochloride

CAS No.17193-40-7 L-4-Nitrophenylalanine methyl ester hydrochloride

CAS No.17193-40-7 L-4-Nitrophenylalanine methyl ester hydrochloride

CAS No.17193-40-7 L-4-Nitrophenylalanine methyl ester hydrochloride

CAS No.17193-40-7 L-4-Nitrophenylalanine methyl ester hydrochloride

CAS No.17193-40-7 L-4-Nitrophenylalanine methyl ester hydrochloride

CAS No.17193-40-7 L-4-Nitrophenylalanine methyl ester hydrochloride

CAS No.17193-40-7 L-4-Nitrophenylalanine methyl ester hydrochloride

CAS No.17193-40-7 L-4-Nitrophenylalanine methyl ester hydrochloride

CAS No.17193-40-7 L-4-Nitrophenylalanine methyl ester hydrochloride

CAS No.17193-40-7 L-4-Nitrophenylalanine methyl ester hydrochloride

CAS No.17193-40-7 L-4-Nitrophenylalanine methyl ester hydrochloride

CAS No.17193-40-7 L-4-Nitrophenylalanine methyl ester hydrochloride

CAS No.17193-40-7 L-4-Nitrophenylalanine methyl ester hydrochloride

CAS No.17193-40-7 L-4-Nitrophenylalanine methyl ester hydrochloride

CAS No.17193-40-7 L-4-Nitrophenylalanine methyl ester hydrochloride

CAS No.17193-40-7 L-4-Nitrophenylalanine methyl ester hydrochloride

CAS No.17193-40-7 L-4-Nitrophenylalanine methyl ester hydrochloride

Reference