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74752-93-5

74752-93-5 | Cyclopropane, 1,1,2,3-tetramethyl-

CAS No: 74752-93-5 Catalog No: AG005HAM MDL No:

Product Description

Catalog Number:
AG005HAM
Chemical Name:
Cyclopropane, 1,1,2,3-tetramethyl-
CAS Number:
74752-93-5
Molecular Formula:
C7H14
Molecular Weight:
98.1861
IUPAC Name:
1,1,2,3-tetramethylcyclopropane
InChI:
InChI=1S/C7H14/c1-5-6(2)7(5,3)4/h5-6H,1-4H3
InChI Key:
ZASOSNWAQIGWQT-UHFFFAOYSA-N
SMILES:
CC1C(C1(C)C)C

Properties

Complexity:
72  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
98.11g/mol
Formal Charge:
0
Heavy Atom Count:
7  
Hydrogen Bond Acceptor Count:
0
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
98.189g/mol
Monoisotopic Mass:
98.11g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
0A^2
Undefined Atom Stereocenter Count:
2  
Undefined Bond Stereocenter Count:
0
XLogP3:
2.8  

Literature

Title Journal
Synthesis and anticonvulsant evaluation of dimethylethanolamine analogues of valproic acid and its tetramethylcyclopropyl analogue. Epilepsy research 20120201
Indol-3-ylcycloalkyl ketones: effects of N1 substituted indole side chain variations on CB(2) cannabinoid receptor activity. Journal of medicinal chemistry 20100114
Tetramethylcyclopropyl analogue of the leading antiepileptic drug, valproic acid: evaluation of the teratogenic effects of its amide derivatives in NMRI mice. Birth defects research. Part A, Clinical and molecular teratology 20080901
Modifications of antiepileptic drugs for improved tolerability and efficacy. Perspectives in medicinal chemistry 20080101
Preclinical evaluation of 2,2,3,3-tetramethylcyclopropanecarbonyl-urea, a novel, second generation to valproic acid, antiepileptic drug. Neuropharmacology 20060901
Efficacy of antiepileptic tetramethylcyclopropyl analogues of valproic acid amides in a rat model of neuropathic pain. Neuropharmacology 20051201
Tetramethylcyclopropyl analogue of a leading antiepileptic drug, valproic acid. Synthesis and evaluation of anticonvulsant activity of its amide derivatives. Journal of medicinal chemistry 20040812

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