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tert-butyl ((4,4-dibromo-2-methylbut-3-en-1-yl)oxy)diphenylsilane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

337375-99-2

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337375-99-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 337375-99-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,7,3,7 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 337375-99:
(8*3)+(7*3)+(6*7)+(5*3)+(4*7)+(3*5)+(2*9)+(1*9)=172
172 % 10 = 2
So 337375-99-2 is a valid CAS Registry Number.

337375-99-2Relevant articles and documents

Progress toward the total synthesis of saudin: Development of a tandem Stille-oxa-electrocyclization reaction

Tambar, Uttam K.,Kano, Taichi,Stoltz, Brian M.

, p. 2413 - 2416 (2005)

(Chemical Equation Presented) A diastereoselective tandem Stille-oxa-electrocyclization reaction provides access to the core of the diterpenoid natural product saudin. Additionally, this new reaction sequence was extended to the convergent preparation of

INDOLE DERIVATIVES AS ALPHA-1 -ANTITRYPSIN MODULATORS FOR TREATING ALPHA-1 -ANTITRYPSIN DEFICIENCY (AATD)

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Paragraph 00234; 00316; 00778; 00781, (2021/10/11)

Indole derivatives as alpha-l-antitrypsin modulators for treating alpha-l-antitrypsin deficiency (AATD).

Convergent and diastereoselective synthesis of the polycyclic pyran core of saudin

Tambar, Uttam K.,Kano, Taichi,Zepernick, John F.,Stoltz, Brian M.

, p. 8357 - 8364 (2007/10/03)

The natural product saudin was found to induce hypoglycemia in mice and, therefore, could be an appealing lead structure for the development of new agents to treat diabetes. A diastereoselective tandem Stilleoxa- electrocyclization reaction has been devel

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