45766-35-6 Usage
General Description
2,3-dihydro-1H-isoindol-5-amine is a chemical compound that belongs to the isoindoline class of chemicals. It is a heterocyclic amine with a molecular formula of C8H9N. 2,3-DIHYDRO-1H-ISOINDOL-5-AMINE is synthesized through various organic reactions and is used in the production of pharmaceuticals, agrochemicals, and other organic compounds. It has potential applications in the development of various drugs due to its unique structure and properties. Additionally, it is used as a building block in the production of specialty chemicals and can also act as a versatile intermediate in organic synthesis. Overall, 2,3-dihydro-1H-isoindol-5-amine has potential industrial and pharmaceutical applications and is a key component in the synthesis of various organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 45766-35-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,5,7,6 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 45766-35:
(7*4)+(6*5)+(5*7)+(4*6)+(3*6)+(2*3)+(1*5)=146
146 % 10 = 6
So 45766-35-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H10N2/c9-8-2-1-6-4-10-5-7(6)3-8/h1-3,10H,4-5,9H2
45766-35-6Relevant articles and documents
Potent non-hydroxamate inhibitors of histone deacetylase-8: Role and scope of an isoindolin-2-yl linker with an α-amino amide as the zinc-binding unit
Chan, A. W. Edith,Greenwood, Simon O. R.,Hansen, D. Flemming,Marson, Charles M.
, (2020/01/22)
A series of potent inhibitors of histone deacetylase-8 (HDAC8) is described that contains an α-amino amide zinc-binding unit and a substituted isoindolinyl capping group. The presence of a 2,4-dichlorophenyl unit located in the acetate-release cavity was
Isoindoline derivative
-
, (2008/06/13)
Isoindoline derivatives represented by the formula (I) and their salts are disclosed. STR1 There are many varieties for the compound depending on the types of residues R1 -R9 and X. The compounds can be prepared from quinoline derivatives of the formula (II) and an isoindoline derivatives of the formula (III). The compounds of formula (I) and their salts have excellent antibacterial activities against both gram positive and gram negative microorganisms. They can be used as a medicine, an agrichemical, and a food preservative.
