465-73-6 Usage
Chemical Properties
Crystals.
Uses
Insecticide.
General Description
Solid. ISODRIN is no longer used as a pesticide. Isomer of aldrin.
Reactivity Profile
ISODRIN is related to aldrin. (nonspecific -- Aldrin) When heated to decomposition ISODRIN emits toxic fumes of chlorine. Unstable, reactions induced by light or acid. [EPA, 1998].
Hazard
Toxic, use may be restricted.
Health Hazard
ISODRIN is classified as extremely toxic. Probable oral lethal dose for humans is 5-50 mg/kg or between 7 drops and 1 teaspoonful for a 70 kg (150 lb.) person. It causes renal damage and hyperactivity of sympathetic nervous system.
Fire Hazard
(Non-Specific -- Aldrin) ISODRIN may burn but may not ignite readily. Container may explode in heat of fire. Fire and runoff from fire control water may produce irritating or poisonous gases. Material is related to aldrin. (Non-Specific -- Aldrin) When heated to decomposition ISODRIN emits toxic fumes of chlorine. Unstable, reactions induced by light or acid.
Check Digit Verification of cas no
The CAS Registry Mumber 465-73-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,6 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 465-73:
(5*4)+(4*6)+(3*5)+(2*7)+(1*3)=76
76 % 10 = 6
So 465-73-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H8Cl6/c13-8-9(14)11(16)7-5-2-1-4(3-5)6(7)10(8,15)12(11,17)18/h1-2,4-7H,3H2/t4-,5+,6-,7+,10-,11+
465-73-6Relevant articles and documents
CYCLOADDITIONS OF HEXACHLOROCYCLOPENTADIENE TO 7-SUBSTITUTED NORBORNADIENES: REMOTE SUBSTITUENT EFFECTS ON REACTIVITY AND STEREOSELECTIVITY
Houk, K. N.,Mueller, Paul H.,Wu, Yun-Dong,Mazzocchi, Paul H.,Shook, David,Khachik, Frederick
, p. 7285 - 7288 (2007/10/02)
The rates and stereoselectivities of the cycloadditions of hexachlorocyclopentadiene to norbornadienes substituted at the 7-position by tert-butyl, trimethylsilyl, methoxy, acetoxy, hydroxy, methoxymethyl, and methoxycarbonyl groups have been measured.The rates correlate with substituent electronegativities.