7168-55-0 Usage
General Description
1,1'-Biphenyl, 2,2'-dimethoxy-5,5'-dimethyl- is a chemical compound with the formula C18H20O2. It is a biphenyl derivative with two methoxy and two methyl groups attached to the aromatic rings. 1,1'-Biphenyl, 2,2'-dimethoxy-5,5'-dimethyl- is commonly used as a building block in organic synthesis and in the production of pharmaceuticals, agrochemicals, and other fine chemicals. It is also known for its use as a starting material in the synthesis of various organic compounds and has been investigated for its potential pharmacological properties. However, due to its limited commercial availability and high cost, its use is somewhat restricted. Overall, 1,1'-Biphenyl, 2,2'-dimethoxy-5,5'-dimethyl- is a versatile compound with various potential applications in the field of organic chemistry and chemical synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 7168-55-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,6 and 8 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7168-55:
(6*7)+(5*1)+(4*6)+(3*8)+(2*5)+(1*5)=110
110 % 10 = 0
So 7168-55-0 is a valid CAS Registry Number.
7168-55-0Relevant articles and documents
Inhibition of Enterococcus faecalis biofilm formation by highly active lactones and lactams analogues of rubrolides
Pereira, Ulisses A.,Barbosa, Luiz C.A.,Maltha, Célia R.A.,Demuner, Ant?nio J.,Masood, Mohammed A.,Pimenta, Andréa L.
, p. 127 - 138 (2014/06/23)
Seven β-aryl substituted γ-alkylidene-γ-lactones analogues of rubrolides were synthesized from mucobromic acid and converted through a lactamization with isobutylamine into their corresponding γ-hydroxy- γ-lactams (76-85%). These lactams were converted in
COBALT(II)CHLORIDE CATALYSED ACYLATION OF ANISOLE
Iqbal, Javed,Khan, M. A.,Nayyar, Naresh K.
, p. 5179 - 5182 (2007/10/02)
Cobalt(II)chloride catalysed acylation of anisole with variety of acid chlorides proceeds via an acyl radical to give p-acylated anisoles in good yields.
