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1-Penten-3-ol, 4-(phenylmethoxy)-, (3R,4S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

403694-73-5

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403694-73-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 403694-73-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,3,6,9 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 403694-73:
(8*4)+(7*0)+(6*3)+(5*6)+(4*9)+(3*4)+(2*7)+(1*3)=145
145 % 10 = 5
So 403694-73-5 is a valid CAS Registry Number.

403694-73-5Relevant academic research and scientific papers

De novo synthesis of novel bacterial monosaccharide fusaminic acid

Wei, Ruohan,Liu, Han,Li, Xuechen

, p. 420 - 431 (2019/03/29)

Fusobacterium nucleatum is an oral bacteria related to various types of diseases. As Gram-negative bacteria, lipopolysaccharide (LPS) of Fusobacterium nucleatum could be a potential virulence factor. Recently, the structure of O-antigen in LPS of Fusobact

RCM mediated synthesis of macrosphelides I and G

Sharma, Gangavaram V.M.,Veera Babu, Kagita

, p. 2175 - 2184 (2008/02/11)

The total synthesis of 16-membered macrolides, macraosphelides I and G, has been achieved starting from ethyl-(S)-lactate and (S)-malic acid. A combination of Jacobsen's hydrolytic kinetic resolution and Sharpless epoxidation is used for the creation of two stereogenic centres, while Yamaguchi esterification and ring-closing metathesis strategies were used for the construction of the lactone ring.

Asymmetric total synthesis of (+)-brefeldin A from (S)-lactate by triple chirality transfer process and nitrile oxide cycloaddition

Kim, Deukjoon,Lee, Jongkook,Phil, Jong Shim,Joong, Inn Lim,Jo, Hyunil,Kim, Sanghee

, p. 764 - 771 (2007/10/03)

A novel synthesis of (+)-brefeldin A (1) has been accomplished on the basis of triple chirality transfer methodology, intramolecular ester enolate alkylation, and both intra- and intermolecular nitrile oxide cycloaddition strategies.

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