1135822-19-3 Usage
General Description
2-(diethylcarbamoyloxy)-3,5-dimethoxyphenylboronic acid is a chemical compound with the molecular formula C17H26BNO6. It is an organoboron compound that is commonly used in organic synthesis as a reagent for cross-coupling reactions. It is also known as a potent inhibitor of serine proteases and has potential applications in pharmaceutical research and drug development. The compound is a white to off-white powder that is sparingly soluble in water, but soluble in organic solvents such as acetone and methanol. It is important to handle this compound with caution, as it may be harmful if ingested, inhaled, or comes into contact with the skin.
Check Digit Verification of cas no
The CAS Registry Mumber 1135822-19-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,3,5,8,2 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1135822-19:
(9*1)+(8*1)+(7*3)+(6*5)+(5*8)+(4*2)+(3*2)+(2*1)+(1*9)=133
133 % 10 = 3
So 1135822-19-3 is a valid CAS Registry Number.
1135822-19-3Relevant articles and documents
Combined metalation-cross coupling strategies: A synthesis of schumanniophytine by a key biaryl O-carbamate remote anionic fries rearrangement
Macklin, Todd K.,Reed, Mark A.,Snieckus, Victor
supporting information; scheme or table, p. 1507 - 1509 (2009/04/11)
A short synthesis of the alkaloid schumanniophytine (1) starting from simple building blocks and involving directed ortho metalation (DoM), Suzuki-Miyaura cross coupling, and a key ortho-silicon-induced O-carbamate remote anionic Fries rearrangement (3) is described. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.
