61716-00-5 Usage
Description
Methylene-2-azido-6-benzylaminopurine is a chemical compound that belongs to the family of azido compounds and is derived from the purine base. It is commonly used in the field of biochemistry and molecular biology as a potent and selective inhibitor of cytokinin oxidase/dehydrogenase, an enzyme involved in the degradation of cytokinins, which are plant hormones involved in cell division, shoot initiation, and other aspects of plant growth.
Uses
Used in Biochemistry and Molecular Biology:
Methylene-2-azido-6-benzylaminopurine is used as a potent and selective inhibitor of cytokinin oxidase/dehydrogenase for studying the role of cytokinins in plant growth and development.
Used in Agricultural Industry:
Methylene-2-azido-6-benzylaminopurine is used as a plant growth promoter to enhance crop yield and improve overall plant growth.
Used in Pharmaceutical Research:
Methylene-2-azido-6-benzylaminopurine is used as a potential medicinal agent for various human health conditions due to its unique chemical properties and biological activity.
Check Digit Verification of cas no
The CAS Registry Mumber 61716-00-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,7,1 and 6 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 61716-00:
(7*6)+(6*1)+(5*7)+(4*1)+(3*6)+(2*0)+(1*0)=105
105 % 10 = 5
So 61716-00-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H10N8/c13-20-19-12-17-10(9-11(18-12)16-7-15-9)14-6-8-4-2-1-3-5-8/h1-5,7H,6H2,(H2,14,15,16,17,18)
61716-00-5Relevant articles and documents
Facile synthesis of 8-azido-6-benzylaminopurine
Steklov, Mikhail Yu.,Tararov, Vitali I.,Romanov, Georgy A.,Mikhailov, Sergey N.
, p. 503 - 511 (2011/12/21)
Bromination of 6-benzylaminopurine (1) with Br2 in AcOH in the presence of AcONa afforded 6-benzylamino-8-bromopurine (2) in 59% yield. The position of bromination was confirmed by direct transformation of bromide 2 by reaction with NaN3 in dimethyl sulfoxide to 8-azido-6-benzylaminopurine (3) in a yield of 70% and comparison of its properties with the known compound 2-azido-6- benzylaminopurine (11). Compounds 3 and 11 were checked for their biological activity in specific biotests based on the primary cytokinin effects in living plants. Both synthesized compounds displayed effects similar to the typical cytokinin 6-benzylaminopurine (1). Copyright Taylor and Francis Group, LLC.