60906-78-7 Usage
Uses
Used in Pharmaceutical Industry:
1-(chloromethyl)-2-ethoxy-benzene is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to be incorporated into the molecular structures of drugs, enhancing their therapeutic properties and effectiveness.
Used in Agrochemical Industry:
In the agrochemical sector, 1-(chloromethyl)-2-ethoxy-benzene is utilized as a precursor in the production of agrochemicals, contributing to the development of compounds that can protect crops and enhance agricultural productivity.
Used as a Solvent:
1-(chloromethyl)-2-ethoxy-benzene is employed as a solvent in various chemical processes due to its ability to dissolve a wide range of substances, facilitating reactions and improving the efficiency of chemical synthesis.
Used in Organic Synthesis:
As an intermediate in organic synthesis, 1-(chloromethyl)-2-ethoxy-benzene is used for the preparation of a variety of organic compounds, leveraging its reactivity and aromatic nature to construct complex molecular architectures.
Check Digit Verification of cas no
The CAS Registry Mumber 60906-78-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,9,0 and 6 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 60906-78:
(7*6)+(6*0)+(5*9)+(4*0)+(3*6)+(2*7)+(1*8)=127
127 % 10 = 7
So 60906-78-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H11ClO/c1-2-11-9-6-4-3-5-8(9)7-10/h3-6H,2,7H2,1H3
60906-78-7Relevant academic research and scientific papers
High diastereoselectivity in the yang photocyclization via remote hydrogen abstraction reaction
Jang, Mi,Park, Bong Ser
, p. 1509 - 1514 (2016/10/09)
1-Benzoyl-1-(o-alkoxyphenyl)cyclopropanes undergo Yang photocyclization to form dihydrobenzopyranols in a stereospecific manner. The cyclopropyl group at alpha position to carbonyls gives not only a bias in the most stable geometries of the starting ketones but also conformational restriction on geometries of biradical intermediates. More importantly, intramolecular hydrogen bonds seem to give an additional effect on conformational control of the biradical reactivity.
PIPERAZINE DERIVATIVES WHICH EXHIBIT ACTIVITY AS SEROTONIN AND NORADRENALINE RE-UPATKE INHIBITORS
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Page/Page column 47, (2010/02/13)
A compound of formula (I), wherein R1 is H; R2 is aryl, het, C3-8cycloalkyl, C1-6alkyl, (CH2)zaryl or R4, wherein each of the cycloalkyl, aryl, het and R4 groups is op
