56276-06-3 Usage
Molecular Weight
163.19 g/mol The molecular weight is the mass of one mole of the compound, calculated by adding the atomic weights of all the atoms in the molecular formula.
Appearance
White to off-white crystalline solid This describes the physical appearance of the compound.
Odor
Faint, floral This describes the smell of the compound.
Chemical Structure
An indole ring and a propanol group This describes the arrangement of atoms in the compound, consisting of an indole ring and a propanol group.
Usage
Fragrance ingredient in cosmetics, soaps, and personal care products This describes the common use of the compound in various products.
Antimicrobial Properties
Exhibits antimicrobial properties This describes the ability of the compound to kill or inhibit the growth of microorganisms.
Potential Applications
Pharmaceutical and agricultural industries This describes the potential use of the compound in these industries.
Therapeutic Potential
Studied for its potential use as a therapeutic agent in the treatment of various diseases This describes the potential use of the compound as a medicine to treat different diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 56276-06-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,2,7 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 56276-06:
(7*5)+(6*6)+(5*2)+(4*7)+(3*6)+(2*0)+(1*6)=133
133 % 10 = 3
So 56276-06-3 is a valid CAS Registry Number.
56276-06-3Relevant articles and documents
A one-pot access to cycloalkano[1,2-a]indoles through an intramolecular alkyl migration reaction in indolylborates
Ishikura, Minoru,Ida, Wataru,Yanada, Kazuo
, p. 1015 - 1024 (2006)
A novel one-pot protocol for the preparation of cycloalkano[1,2-a]indoles by way of an intramolecular alkyl migration reaction in cyclic indolylborates is described. NaOMe was found to act as a successful trialkylboryl-protecting group against to the lithiation at the C2 of the indole ring. Treatment of cyclic indolylborates with electrophiles produced cycloalkano-[1,2-a]indoles.
