Cas no 22888-60-4 (L-Histidine, methylester, hydrochloride (1:?))
22888-60-4 structure
Product Name:L-Histidine, methylester, hydrochloride (1:?)
CAS No:22888-60-4
MF:C7H12ClN3O2
MW:205.642080307007
CID:283952
PubChem ID:12658397
Update Time:2025-04-19
L-Histidine, methylester, hydrochloride (1:?) Chemical and Physical Properties
Names and Identifiers
-
- L-Histidine, methylester, hydrochloride (1:?)
- methyl (2S)-2-amino-3-(1H-imidazol-5-yl)propanoate,hydrochloride
- methyl (2S)-2-amino-3-(1H-imidazol-4-yl)propanoate hydrochloride
- Methyl L-histidinate HCl
- Methyl L-histidinate hydrochloride
- L-histidine methyl ester hydrochloride
- methyl (2S)-2-amino-3-(1H-imidazol-5-yl)propanoate;hydrochloride
- 18684-16-7
- SCHEMBL1375315
- AC8660
- L-Histidine, Methyl ester, Monohydrochloride
- VEEIFXWJNCAVEQ-RGMNGODLSA-N
- Histidine methyl ester hydrochloride
- EN300-118950
- NS00083034
- (S)-METHYL 2-AMINO-3-(1H-IMIDAZOL-5-YL)PROPANOATE 2HCL
- Methyl histidinate--hydrogen chloride (1/1)
- DTXSID20945565
- methyl (2S)-2-amino-3-(1H-imidazol-5-yl)propanoate hydrochloride
- 22888-60-4
- 7389-87-9
- EINECS 245-300-4
-
- Inchi： 1S/C7H11N3O2.ClH/c1-12-7(11)6(8)2-5-3-9-4-10-5;/h3-4,6H,2,8H2,1H3,(H,9,10);1H/t6-;/m0./s1
- InChI Key： VEEIFXWJNCAVEQ-RGMNGODLSA-N
- SMILES： Cl.O(C)C([C@H](CC1=CN=CN1)N)=O
Computed Properties
- Exact Mass: 205.06196
- Monoisotopic Mass: 442.236504
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 6
- Heavy Atom Count: 29
- Rotatable Bond Count: 20
- Complexity: 502
- Covalently-Bonded Unit Count: 2
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 1
- Defined Bond Stereocenter Count: 1
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 112
Experimental Properties
- Boiling Point: 391.1°C at 760 mmHg
- Flash Point: 190.3°C
- PSA: 81
L-Histidine, methylester, hydrochloride (1:?) Related Literature
-
1. The interaction of L-(+)-histidine methyl ester with metal ions. Part II. The metal-ion catalysed base hydrolysis of L-(+)-histidine methyl esterR. W. Hay,P. J. Morris J. Chem. Soc. A 1971 1524
-
2. Further studies on the protection of histidine side chains in peptide synthesis: the use of the π-benzyloxymethyl groupTom Brown,John H. Jones,John D. Richards J. Chem. Soc. Perkin Trans. 1 1982 1553
-
3. Peptide-bond formation, chemoselective acylation of amino acids, and crosslinking reaction between amino acids utilizing a functional five-membered heterocycle, 1,3-thiazolidine-2-thioneYoshimitsu Nagao,Tadayo Miyasaka,Kaoru Seno,Eiichi Fujita,Daisuke Shibata,Etsushiro Doi J. Chem. Soc. Perkin Trans. 1 1984 2439
22888-60-4 (L-Histidine, methylester, hydrochloride (1:?)) Related Products
- 2098070-20-1(2-(3-(Pyridin-3-yl)-1H-pyrazol-1-yl)acetimidamide)
- 2680771-01-9(4-cyclopentyl-3-{(prop-2-en-1-yloxy)carbonylamino}butanoic acid)
- 1444113-98-7(N-(3-cyanothiolan-3-yl)-2-[(2,2,2-trifluoroethyl)sulfanyl]pyridine-4-carboxamide)
- 332062-08-5(Fmoc-S-3-amino-4,4-diphenyl-butyric acid)
- 1270529-38-8(1,2,3,4,5,6-Hexahydro-[2,3]bipyridinyl-6-ol)
- 941977-17-9(N'-(3-chloro-2-methylphenyl)-N-2-(dimethylamino)-2-(naphthalen-1-yl)ethylethanediamide)
- 2138166-62-6(2,2-Difluoro-3-[methyl(2-methylbutyl)amino]propanoic acid)
- 89640-58-4(2-Iodo-4-nitrophenylhydrazine)
- 1449132-38-0(3-Fluoro-5-(2-fluoro-5-methylbenzylcarbamoyl)benzeneboronic acid)
- 2034271-14-0(2-(1H-indol-3-yl)-N-{[6-(thiophen-2-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl]methyl}acetamide)
Recommended suppliers
Nanjing jingzhu bio-technology Co., Ltd.
Gold Member
Audited Supplier
CN Supplier
Bulk
Shenzhen GeneSeqTools Bioscience & Technology Co. Ltd.
Gold Member
Audited Supplier
CN Supplier
Reagent
Beyond Pharmaceutical Co., Ltd
Gold Member
Audited Supplier
CN Supplier
Reagent
上海嶸奧生物技術(shù)有限公司
Gold Member
Audited Supplier
CN Supplier
Reagent
Wuhan ChemNorm Biotech Co.,Ltd.
Gold Member
Audited Supplier
CN Supplier
Reagent
