71445-20-0 Usage
General Description
1-[2-(Z)-Methoxyimino-2-(2-aminothiazol-4-yl)acetoxy]benzotrizole is a chemical compound with potential biological and pharmaceutical applications. It is a derivative of benzotriazole and contains an oxime and thiazole functional group. The compound has been studied for its potential antimicrobial and antifungal properties, as well as its ability to inhibit the growth of certain cancer cells. Additionally, it has shown potential as a photostabilizer in sunscreens and other personal care products, as it absorbs and dissipates UV radiation. The unique structure and functional groups of 1-[2-(Z)-Methoxyimino-2-(2-aminothiazol-4-yl)acetoxy]benzotrizole make it a versatile and valuable compound in various fields of research and industry.
Check Digit Verification of cas no
The CAS Registry Mumber 71445-20-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,4,4 and 5 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 71445-20:
(7*7)+(6*1)+(5*4)+(4*4)+(3*5)+(2*2)+(1*0)=110
110 % 10 = 0
So 71445-20-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H10N6O3S/c1-20-16-10(8-6-22-12(13)14-8)11(19)21-18-9-5-3-2-4-7(9)15-17-18/h2-6H,1H3,(H2,13,14)/b16-10-
71445-20-0Relevant articles and documents
Synthesis and structure-activity relationship of C-3 substituted triazolylthiomethyl cephems
Singh,Fiakpui,Galpin,Stewart,Singh,Micetich
, p. 301 - 309 (2007/10/03)
A series of C-3 substituted triazolylthiomethyl cephems with an aminothiazolemethoxyiminoacetamido side chain at C-7 were synthesized and tested for antimicrobial activity against clinically-relevant isolates. The compound with 3-pyridyl at C-5 and methyl at N-4 of the triazole moiety exhibited good antibacterial activity against both Gram-positive and Gram-negative bacteria, with the exception of pseudomonas spp against which none of the derivatives exhibited favorable activity.
Synthesis and antibacterial activities of 2-oxaisocephems
Tsubouchi,Tsuji,Yasumura,Ishikawa
, p. 2084 - 2089 (2007/10/02)
A series of 2-oxaisocephems with a thio-substituted methyl group at the 3-position and a 2-aminothiazol-4-yl moiety at the 7-position was synthesized via benzyl 3-acetyloxymethyl-7-azido-8-oxo-1-aza-4-oxabicyclo[4.2.0]oct-2-ene-2-c arboxylate (2), derived
