1158734-28-1 Usage
Uses
Used in Organic Synthesis:
1,4-Di(hydroxyMethyl)benzene-d4 is used as a synthetic building block for the creation of various organic compounds. The deuterium atoms in the molecule can enhance the stability and reactivity of the compound, making it a valuable asset in the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
1,4-Di(hydroxyMethyl)benzene-d4 is used as a starting material for the development of new pharmaceutical compounds. The deuterium substitution can improve the pharmacokinetic properties of the resulting drugs, such as their absorption, distribution, metabolism, and excretion, potentially leading to more effective and safer medications.
Used in Chemical Research:
1,4-Di(hydroxyMethyl)benzene-d4 is used as a research tool in the field of chemistry. The deuterated compound can be employed in various experimental setups to study the effects of deuterium substitution on reaction mechanisms, kinetics, and product formation.
Used in Material Science:
1,4-Di(hydroxyMethyl)benzene-d4 can be used as a component in the development of novel materials with specific properties. The deuterium atoms in the molecule can influence the material's physical and chemical characteristics, such as its thermal stability, mechanical strength, and electrical conductivity.
Check Digit Verification of cas no
The CAS Registry Mumber 1158734-28-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,8,7,3 and 4 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1158734-28:
(9*1)+(8*1)+(7*5)+(6*8)+(5*7)+(4*3)+(3*4)+(2*2)+(1*8)=171
171 % 10 = 1
So 1158734-28-1 is a valid CAS Registry Number.
1158734-28-1Relevant articles and documents
Novel Transannular Reactions in the Acid Hydrolysis of Diazotized syn- and anti-4-Amino(1,4)naphthalenoparacyclophanes
Takada, Yoshihiro,Tsuchiya, Kazuhiko,Takahashi, Senji,Mori, Nobuo
, p. 2141 - 2145 (2007/10/02)
The diazonium ions derived from the title syn- and anti-4-aminocyclophanes 1a und 4a in aqueous solution undergo transannular reactions to give 17-hydroxy(1,4)naphthalenoparacyclophane 3a and 9,10-dihydro-1,9:4,10-diethano-9,10-ethenoanthracene 6a, respectively.Deuterium-tracer experiments suggest that the reaction of diazotized 1a proceeds via a pathway involving tranannular diazo coupling followed by generation of a 16,17-didehydro intermediate.On the other hand, the reaction pathway of diazotized 4a involves dediazonization followed by transannular electrophilic addition.
