2612-56-8 Usage
Uses
Used in Pharmaceutical Industry:
3 4-Diethoxytoluene 96 is used as an intermediate in the synthesis of various pharmaceutical compounds, contributing to the development of new drugs and medications.
Used in Perfumery and Cosmetics Industry:
3 4-Diethoxytoluene 96 is used as a fragrance ingredient in perfumes and cosmetics, enhancing the scent profiles of these products and providing a pleasant fruity aroma.
Used in Specialty Chemicals Industry:
3 4-Diethoxytoluene 96 is used as a solvent for organic reactions, facilitating various chemical processes and reactions in the specialty chemicals sector.
Used in Research and Laboratory Settings:
3 4-Diethoxytoluene 96 is used as a reagent and a reference standard in research and laboratory settings, aiding in the analysis and standardization of chemical processes and experiments.
Check Digit Verification of cas no
The CAS Registry Mumber 2612-56-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,1 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2612-56:
(6*2)+(5*6)+(4*1)+(3*2)+(2*5)+(1*6)=68
68 % 10 = 8
So 2612-56-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H16O2/c1-4-12-10-7-6-9(3)8-11(10)13-5-2/h6-8H,4-5H2,1-3H3
2612-56-8Relevant academic research and scientific papers
A solvent-controlled highly efficient Pd-C catalyzed hydrogenolysis of benzaldehydes to methylbenzenes via a novel 'acetal pathway'
Xing, Lixin,Wang, Xinyan,Cheng, Chuanjie,Zhu, Rui,Liu, Bo,Hu, Yuefei
, p. 9382 - 9386 (2008/02/10)
Pd-C catalyzed hydrogenolysis of benzaldehydes to methylbenzenes has been described to proceed via a 'benzenemethanol pathway'. In this article, a novel 'acetal pathway' was first revealed by a systematic study when lower alcohols were used as solvents and a solvent-controlled highly efficient procedure was established.
Process for substituted 5-benzyl-2,4-diamino-pyrimidines
-
, (2008/06/13)
A process for preparing a compound of the formula STR1 wherein R1 and R2 are lower alkoxy or taken together are METHYLENEDIOXY; R3 is lower alkyl or hydrogen, which comprises the step of reacting an aromatic compound of the formula STR2 wherein R1, R2 and R3 are as previously described, with a diamino-pyrimidine of the formula STR3 wherein R4 is lower alkoxy, benzyloxy, hydroxy or halogen, in the presence of an inorganic or organic acid selected from the group consisting of ortho-phosphoric acid, poly-phosphoric acid, hydrohalic acids and tri-haloacetic acids, at a temperature in the range of from about 50° C. to about 110° C., is described.
