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910581-09-8

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910581-09-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 910581-09-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,0,5,8 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 910581-09:
(8*9)+(7*1)+(6*0)+(5*5)+(4*8)+(3*1)+(2*0)+(1*9)=148
148 % 10 = 8
So 910581-09-8 is a valid CAS Registry Number.

910581-09-8Relevant academic research and scientific papers

Enantioselective Synthesis of the Sex Pheromone of Lichen Moth, Miltochrista calamine, and Its Diastereomer

Yuan, Gucheng,Liu, Jiawei,Yu, Shihang,Wang, Xueyang,Bian, Qinghua,Wang, Min,Zhong, Jiangchun

supporting information, p. 80 - 83 (2021/10/05)

The synthesis of a Miltochrista calamine sex pheromone and its diastereomer has been developed. The key steps of the synthetic approach involved Evans' chiral auxiliaries and the addition of alkyne to aldehyde, which were firstly applied to prepare this sex pheromone and its diastereomer. The synthetic sex pheromone could be used to trap insects and study physiological and ecological questions of the lichen moth.

"Click" synthesis of small molecule probes for activity-based fingerprinting of matrix metalloproteases

Wang, Jun,Uttamchandani, Mahesh,Li, Junqi,Hu, Mingyu,Yao, Shao Q.

, p. 3783 - 3785 (2007/10/03)

By using "Click Chemistry", we achieved the facile synthesis of various affinity-based hydroxamate probes that enable generation of activity-based fingerprints of a variety of metalloproteases, including matrix metalloproteases (MMPs), in proteomics experiments. The Royal Society of Chemistry 2006.

Rapid assembly of matrix metalloprotease inhibitors using click chemistry

Wang, Jun,Uttamchandani, Mahesh,Li, Junqi,Hu, Mingyu,Yao, Shao Q.

, p. 3821 - 3824 (2007/10/03)

A panel of 96 metalloprotease inhibitors was assembled using "click chemistry" by reacting eight zinc-binding hydroxamate warheads with 12 azide building blocks. Screens of the bidentate compounds against representative metalloproteases provided discerning inhibition fingerprints, revealing compounds with low micromolar potency against MMP-7. The relative ease and convenience of the strategy in constructing focused chemical libraries for rapid in situ screening of MMPs is thereby demonstrated.

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