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2-benzyloxyl-4-methoxyphenylacetic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74235-36-2

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74235-36-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74235-36-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,2,3 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 74235-36:
(7*7)+(6*4)+(5*2)+(4*3)+(3*5)+(2*3)+(1*6)=122
122 % 10 = 2
So 74235-36-2 is a valid CAS Registry Number.

74235-36-2Relevant academic research and scientific papers

MEDICARPIN, ITS DERIVATIVES, MANUFACTURING METHOD THEREOF

-

, (2018/04/20)

A compound and a method thereof are provided. The compound of the invention has formula I shown below. Each variable in formula I and manufacturing method are defined in the specification. The invention also provides a method for treating organ dysfunction.

Total Synthesis of (+)-Medicarpin

Yang, Xiaoming,Zhao, Yu,Hsieh, Min-Tsang,Xin, Guang,Wu, Rong-Tsun,Hsu, Pei-Lun,Horng, Lin-Yea,Sung, Hui-Ching,Cheng, Chien-Hsin,Lee, Kuo-Hsiung

, p. 3284 - 3288 (2018/01/02)

(+)-Medicarpin has been synthesized asymmetrically for the first time in a linear scalable process with an overall yield of 11%. The two chiral centers were constructed in one step via condensation using a chiral oxazolidinone auxiliary. This method will likely accelerate research on medicarpin as an erythropoietin inducer for erythropoietin-deficient diseases.

Synthesis of tetracyclic heterocompounds as selective estrogen receptor modulators. Part 1. Process development for scale-up of 2,5,8-substituted 5,11 -dihydrochromeno[4,3-c]chromene derivatives

Li, Xun,Reuman, Michael,Russell, Ronald K.,Adams, Richard,Ma, Robert,Beish, Sandra,Branum, Shawn,Youells, Scott,Roberts, Jerry,Jain, Nareshkumar,Kanojia, Ramesh,Sui, Zhihua

, p. 414 - 421 (2012/12/31)

Unsymmetrical benzopyranobenzopyran compounds are novel selective estrogen receptor modulators (SERMs). A reproducible and nonchromatographic process was developed to prepare multihundred gram quantities of 5-(4-(2-(piperidin-1-yl) ethoxy)-phenyl)-5,11-di

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