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2-(2-fluoro-4-hydroxy-5-methoxyphenyl)acetic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

140146-47-0

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140146-47-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 140146-47-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,1,4 and 6 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 140146-47:
(8*1)+(7*4)+(6*0)+(5*1)+(4*4)+(3*6)+(2*4)+(1*7)=90
90 % 10 = 0
So 140146-47-0 is a valid CAS Registry Number.

140146-47-0Downstream Products

140146-47-0Relevant academic research and scientific papers

Phenyl-fluoride substituted phenylacetic acid ester compound and use thereof

-

, (2017/11/17)

The invention relates to a phenyl-fluoride substituted phenylacetate compound shown as a general formula (I), a pharmaceutical composition containing the same and application thereof to anesthesia, sedation and analgesia.

Phenyl acetate derivatives, fluorine-substituted on the phenyl group, as rapid recovery hypnotic agents with reflex depression

Zhang, Heng,Xu, Xiangqing,Chen, Yin,Qiu, Yinli,Liu, Xin,Liu, Bi-Feng,Zhang, Guisen

, p. 524 - 539 (2014/12/11)

We report the synthesis of novel, potentially hypnotic fluorine-substituted phenyl acetate derivatives. We describe the structure-activity relationship that led us to the promising derivative: ethyl 2-(4-(2-(diethylamino)-2-oxoethoxy)-5-ethoxy-2-fluorophenyl) acetate (55). The unique pharmacological features of compound 55 are its relatively high affinity for the GABAA receptor, together with a unique affinity for the NMDA receptor, different to propanidid and AZD3043. In animal models, compound 55 showed stronger hypnotic potency and longer duration of LORR than propanidid and AZD3043, but also maintained a rapid recovery time to walking and behavioral recovery. In particular, compound 55 displayed reflex depression during infusion.

SYNTHESIS AND HPLC SEPARATION OF 6-FLUORO-L-DOPA METABOLITES

Luxen, A.,Monclus, M.,Hendrickx, P.-Y.,Masson, C.,Melega, W. P.

, p. 217 - 226 (2007/10/02)

The synthesis of 6-fluoro-L-dopa metabolites (3-O-methyl-6-fluorodopa (1b), 6-fluorodopamine (2a), 3-O-methyl-6-fluorodopamine (2b), 3,4-dihydroxy-6-fluorophenylacetic acid (3a) and 6-fluorohomovanillic acid (3b) is described.A HPLC method for their separ

Synthesis of metabolites of 6-fluoro-DOPA

Nie, Jun-ying,Kirk, Kenneth L.

, p. 259 - 269 (2007/10/02)

Key metabolites of 6-fluoro-DOPA have been prepared by side-chain elaboration of 6-fluorovanillin and 6-fluoroveratraldehyde.

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