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3-chloro-5-[2-chloro-5-(7-oxy-1H-pyrazolo[3,4-b]pyridin-3-ylmethoxy)phenoxy]benzonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1173989-69-9

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1173989-69-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1173989-69-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,3,9,8 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1173989-69:
(9*1)+(8*1)+(7*7)+(6*3)+(5*9)+(4*8)+(3*9)+(2*6)+(1*9)=209
209 % 10 = 9
So 1173989-69-9 is a valid CAS Registry Number.

1173989-69-9Upstream product

1173989-69-9Relevant academic research and scientific papers

Development of a safe and practical N-oxidation procedure using m-CPBA in acetic acid

Alam, Mahbub,Goodyear, Adrian,Scott, Jeremy P.,Vickery, Thomas P.

, p. 443 - 448 (2011)

A safe and practical procedure for the N-oxidation of pyrazolopyridine 4 using meta-chloroperbenzoic acid (m-CPBA) in acetic acid is described. Key safety experiments are outlined which have led to the development and implementation of this reaction on 28-kg scale in 98% isolated yield.

Development of practical syntheses of potent non-nucleoside reverse transcriptase inhibitors

Kuethe, Jeffrey T.,Zhong, Yong-Li,Alam, Mahbub,Alorati, Anthony D.,Beutner, Gregory L.,Cai, Dongwei,Fleitz, Fred J.,Gibb, Andrew D.,Kassim, Amude,Linn, Kathleen,Mancheno, Danny,Marcune, Benjamin,Pye, Philip J.,Scott, Jeremy P.,Tellers, David M.,Xiang, Bangping,Yasuda, Nobuyoshi,Yin, Jingjun,Davies, Ian W.

experimental part, p. 5013 - 5023 (2009/11/30)

The development of practical and efficient syntheses of the potent non-nucleoside reverse transcriptase inhibitors 1 and 2 is described. The preparation of 1 proceeded in four synthetic steps and in 48% overall yield from 3. The long-term synthesis of 2 proceeded in nine synthetic steps and in 47% overall yield from commercially available 2,6-diflurorpyridine. The route to 2 was highlighted by the three-step synthesis of intermediate 22 and the high yielding coupling between 18 and phenol 8. The overall sequence required no chromatography and has successfully been utilized for the manufacture of 2 on large scale.

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