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63283-42-1

63283-42-1 | 6,7-DIMETHOXY-1-METHYL-1,2,3,4-TETRAHYDROISOQUINOLINE HYDROCHLORIDE, 99

CAS No: 63283-42-1 Catalog No: AG003N17 MDL No:MFCD00050647

Product Description

Catalog Number:
AG003N17
Chemical Name:
6,7-DIMETHOXY-1-METHYL-1,2,3,4-TETRAHYDROISOQUINOLINE HYDROCHLORIDE, 99
CAS Number:
63283-42-1
MDL Number:
MFCD00050647
IUPAC Name:
6,7-dimethoxy-1-methyl-1,2,3,4-tetrahydroisoquinoline;hydrochloride
InChI:
InChI=1S/C12H17NO2.ClH/c1-8-10-7-12(15-3)11(14-2)6-9(10)4-5-13-8;/h6-8,13H,4-5H2,1-3H3;1H
InChI Key:
UJXLTDHDLUBZBL-UHFFFAOYSA-N
NSC Number:
34659

Properties

Complexity:
210  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
2  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
243.103g/mol
Formal Charge:
0
Heavy Atom Count:
16  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
243.731g/mol
Monoisotopic Mass:
243.103g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
30.5A^2
Undefined Atom Stereocenter Count:
1  
Undefined Bond Stereocenter Count:
0

Literature

Title Journal
Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis. Bioorganic & medicinal chemistry letters 20101101
Role of acetaldehyde in tobacco smoke addiction. European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology 20071001
Microsphere-based protease assays and screening application for lethal factor and factor Xa. Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501
[Asymmetric reactions based on activation and structure control of molecule--asymmetric reaction of lithiated nucleophiles]. Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan 20040201
Tetrahydroisoquinoline and beta-carboline alkaloids from Haloxylon articulatum (Cav.) Bunge (Chenopodiaceae). Zeitschrift fur Naturforschung. C, Journal of biosciences 20030101

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