67386-38-3 Usage
Uses
Used in Pharmaceutical Industry:
2-Phenoxyacetamidine hydrochloride is used as an antihistamine agent for the treatment of allergies and allergic reactions. It is employed to alleviate symptoms caused by the release of histamine in the body, such as itching, sneezing, and runny nose, by blocking the histamine's action.
Used in Medical Treatments:
2-Phenoxyacetamidine hydrochloride is used as a therapeutic agent to manage allergic conditions. It is administered in forms such as tablets or injections to ensure effective delivery of the compound to the patient, aiming to provide relief from allergic symptoms while being generally well-tolerated.
Check Digit Verification of cas no
The CAS Registry Mumber 67386-38-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,3,8 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 67386-38:
(7*6)+(6*7)+(5*3)+(4*8)+(3*6)+(2*3)+(1*8)=163
163 % 10 = 3
So 67386-38-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H10N2O.ClH/c9-8(10)6-11-7-4-2-1-3-5-7;/h1-5H,6H2,(H3,9,10);1H
67386-38-3Relevant academic research and scientific papers
Kinetics of alkylhalocarbene rearrangements: Modulation by fluorine substituents
Moss, Robert A.,Ho, Guo-Jie,Liu, Weiguo
, p. 959 - 963 (2007/10/02)
Rate constants were measured by laser flash photolytic methods for hydrogen and carbon 1,2-migrations in four different alkylchlorocarbenes and in the analogous alkylfluorocarbenes. The carbenes, products, and rate constants (-1 were as follows
EFFECT OF REMOTE HETEROATOM SUBSTITUENTS ON STEREOCHEMISTRY IN 1,2 H MIGRATION TO DIVALENT CARBON. EVIDENCE FOR " NEGATIVE " HYPERCONJUGATION OF CARBENE LONE PAIR
Tomioka, Hideo,Hayashi, Norihiro,Inoue, Noboru,Izawa, Yasuji
, p. 1651 - 1654 (2007/10/02)
Aryloxymethylchlorocarbene generated by photolysis of the corresponding diazirine afforded α-aryloxy-β-chloroalkene.The thermodynamically less stable Z-products are the major isomers and its content becomes dominant as more electron-withdrawing groups are
