13375-88-7 Usage
Physical State
Colorless liquid
Solubility
Insoluble in water
Vapor Pressure
Very low
Primary Uses
a. Solvent in industrial applications
b. Production processes for chemicals and pharmaceuticals
c. Intermediate in the synthesis of other compounds
d. Pesticide
Health Hazards
a. Harmful if inhaled (respiratory system irritation)
b. Potentially harmful if ingested
c. Potentially harmful if skin contact occurs
Safety Measures
Handle with care and follow appropriate safety protocols when working with 1,1,1,3-Tetrachloroheptane.
Check Digit Verification of cas no
The CAS Registry Mumber 13375-88-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,7 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13375-88:
(7*1)+(6*3)+(5*3)+(4*7)+(3*5)+(2*8)+(1*8)=107
107 % 10 = 7
So 13375-88-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H12Cl4/c1-2-3-4-6(8)5-7(9,10)11/h6H,2-5H2,1H3
13375-88-7Relevant articles and documents
Addition of CCl4 to olefins catalyzed by chromium and ruthenium complexes: The influence of water as a nucleophilic additive
Khusnutdinov,Schadneva,Oshnyakova,Dzhemilev
experimental part, p. 331 - 338 (2010/06/16)
The feasibility of the addition of CCl4 to linear and cyclic olefins and dienes in the presence of chromium and ruthenium complexes was established. The influence of water as a nucleophilic additive and the influence of the olefin nature, the c
MECHANISM OF THE ADDITION OF TRIBUTYLTIN IODOACETATE TO ALKENES
Degueil-Castaing, M.,Jeso, B. De,Kraus, G. A.,Landgrebe, K.,Maillard, B.
, p. 5927 - 5930 (2007/10/02)
The mechanism of the formation of lactones by free radical additions of tri-n-butyltin iodoacetate to alkenes occurs through a two-step process: a homolytic addition of the ester (addition of .CH2-CO2SnBu3, iodine transfer), followed by a fast ionic cyclization with elimination of tri-n-butyltin iodide.
