51699-43-5 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
A specific brand or trade name given to the compound by a manufacturer or supplier.
Explanation
A diol is a type of alcohol that contains two hydroxyl (OH) groups, which are connected to two different carbon atoms.
Explanation
The compound contains two hydroxyl groups, which contribute to its chemical properties and reactivity.
Explanation
The compound consists of a propanediol backbone with a 3-methylphenyl group attached, which influences its specific chemical properties.
Explanation
The compound is used as a starting material or building block in the synthesis of various polymers and other chemical products.
Explanation
Due to its unique chemical structure and properties, 1,3-Propanediol, 1-(3-methylphenyl)has a wide range of uses in different sectors of the manufacturing industry.
Explanation
The presence of a methyl group attached to a phenyl ring in the compound gives it specific chemical properties that distinguish it from other propanediols.
Type of compound
Diol
Presence of hydroxyl groups
Two
Structure
1,3-Propanediol with a 3-methylphenyl group
Application
Intermediate in the production of polymers and other chemical compounds
Versatility
Various applications in the manufacturing industry
Chemical properties
Influenced by the 3-methylphenyl group
Check Digit Verification of cas no
The CAS Registry Mumber 51699-43-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,6,9 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 51699-43:
(7*5)+(6*1)+(5*6)+(4*9)+(3*9)+(2*4)+(1*3)=145
145 % 10 = 5
So 51699-43-5 is a valid CAS Registry Number.
51699-43-5Relevant articles and documents
Electrocatalytic Activation of Donor–Acceptor Cyclopropanes and Cyclobutanes: An Alternative C(sp3)?C(sp3) Cleavage Mode
Brandt, Felix,Jacob, Christoph R.,Jones, Peter G.,Kolb, Simon,Petzold, Martin,Werz, Daniel B.
supporting information, p. 15928 - 15934 (2021/06/21)
We describe the first electrochemical activation of D–A cyclopropanes and D–A cyclobutanes leading after C(sp3)?C(sp3) cleavage to the formation of highly reactive radical cations. This concept is utilized to formally insert molecula
Synthesis and characterization of a novel liver-targeted prodrug of cytosine-1-β-D-arabinofuranoside monophosphate for the treatment of hepatocellular carcinoma
Boyer, Serge H.,Sun, Zhili,Jiang, Hongjian,Esterbrook, Julie,Gómez-Galeno, Jorge E.,Craigo, William,Reddy, K. Raja,Ugarkar, Bheemarao G.,MacKenna, Deidre A.,Erion, Mark D.
, p. 7711 - 7720 (2007/10/03)
Cytotoxic nucleosides have proven to be ineffective for the treatment of hepatocellular carcinoma (HCC) due, in part, to their inadequate conversion to their active nucleoside triphosphates (NTP) in the liver tumor and high conversion in other tissues. Th
