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38567-00-9

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38567-00-9 Usage

General Description

4-(2-chloro-ethoxy)-benzoic acid methyl ester, also known as methyl 4-(2-chloroethoxy)benzoate, is a chemical compound with the molecular formula C10H11ClO3. It is a colorless to yellow liquid that is used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. 4-(2-CHLORO-ETHOXY)-BENZOIC ACID METHYL ESTER is also a key building block for the production of various ester derivatives that have potential applications in the field of organic chemistry. It is important to handle this chemical with caution, as it can be harmful if ingested, inhaled, or in contact with skin. Additionally, it may cause irritation to the eyes, skin, and respiratory system.

Check Digit Verification of cas no

The CAS Registry Mumber 38567-00-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,5,6 and 7 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 38567-00:
(7*3)+(6*8)+(5*5)+(4*6)+(3*7)+(2*0)+(1*0)=139
139 % 10 = 9
So 38567-00-9 is a valid CAS Registry Number.

38567-00-9Relevant articles and documents

Synthesis and evaluation of raloxifene derivatives as a selective estrogen receptor down-regulator

Shoda, Takuji,Kato, Masashi,Fujisato, Takuma,Misawa, Takashi,Demizu, Yosuke,Inoue, Hideshi,Naito, Mikihiko,Kurihara, Masaaki

, p. 2914 - 2919 (2016)

Estrogen receptors (ERs) play a major role in the growth of human breast cancer cells. A selective estrogen receptor down-regulator (SERD) that acts as not only an inhibitor of ligand binding, but also induces the down-regulation of ER, would be useful fo

Palladium catalyzed chloroethoxylation of aromatic and heteroaromatic chlorides: An orthogonal functionalization of a chloroethoxy linker

Petho, Bálint,Vangel, Dóra,Csenki, János T.,Zwillinger, Márton,Novák, Zoltán

supporting information, p. 4895 - 4899 (2018/07/15)

A novel disconnection based on cross-coupling chemistry was designed to access pharmaceutically relevant aryl-aminoethyl ethers. The developed palladium-catalyzed functionalization of aryl- and heteroaryl chlorides with a sodium tetrakis-(2-chloroethoxy) borate salt is orthogonal to the simple nucleophilic replacement of the chloro function of the ethylene linker. The transformation enables efficient 2-chloroethoxylation in the absence of an additional external base. Subsequent amine substitution of the alkyl halide affords 2-aminoethoxy arenes. The applicability of this method was demonstrated through the synthesis of various aryl- and heteroaryl-alkyl ethers, including the intermediates of marketed drug molecules.

Benzothiophenes and related compounds as estrogen agonists

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Page/Page column 41-42, (2010/02/07)

The invention is a compound of Formula (I): wherein R is —OH, R1is —OH, R2is —H, n is 2 or 3 and X is sulfur, or a pharmaceutically acceptable salt of a compound having Formula (1), or a pharmaceutical composition comprising a compou

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