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4-bromo-3-mercaptobenzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

887507-96-2

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887507-96-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 887507-96-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,7,5,0 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 887507-96:
(8*8)+(7*8)+(6*7)+(5*5)+(4*0)+(3*7)+(2*9)+(1*6)=232
232 % 10 = 2
So 887507-96-2 is a valid CAS Registry Number.

887507-96-2Relevant academic research and scientific papers

Synthesis of multifunctional metal-organic frameworks and tuning the functionalities with pendant ligands

Prasad, Thazhe Kootteri,Suh, Myunghyun Paik

, p. 15034 - 15040 (2020/11/11)

A series of multifunctional metal-organic frameworks (MOFs), SNU-170-SNU-176, has been synthesized using ligands, in which various functional pendants such as -NH2, -SMe, -OMe, -OEt, -OPr, and -OBu are attached to the phenyl ring of 4-(2-carboxyvinyl)benz

Development of a reversible fluorescent probe for reactive sulfur species, sulfane sulfur, and its biological application

Takano, Yoko,Hanaoka, Kenjiro,Shimamoto, Kazuhito,Miyamoto, Ryo,Komatsu, Toru,Ueno, Tasuku,Terai, Takuya,Kimura, Hideo,Nagano, Tetsuo,Urano, Yasuteru

, p. 1064 - 1067 (2017/01/29)

We report a reversible off/on fluorescent probe for monitoring concentration changes of sulfane sulfur by utilizing the unique ability of sulfane sulfur to bind reversibly to other sulfur atoms and the intramolecular spirocyclization reaction of xanthene dyes. It reversibly visualized sulfane sulfur in living A549 cells and primary-cultured hippocampal astrocytes.

TRICYCLIC GUANIDINE DERIVATIVES AS SODIUM-PROTON EXCHANGE INHIBITORS

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Page/Page column 88, (2010/11/30)

Guanidine derivatives having a condensed tricyclic ring of formula 1: are disclosed, wherein U is C(O), CRaRb, O, NRa or S(O)m V is CRaRb or NRa; W is S(O)m ; wherein Ra is H, alkyl, cycloalkyl, alkenyl or aralkyl; Rb is H, alkyl, OH, ORa or OCORa, and m is the integer 0, 1 or 2; R1, R2, R3, R4, R5, R6, R7 and R8 are as defined herein with the proviso that at least one of R1, R2, R3, R4, R5, R6, R7 or R8 is guanidino or guanidino carbonyl. These derivatives are sodium-proton exchange inhibitors and are useful as medicaments for the treatment of, for example, organ disorders associated with ischemia and reperfusion, cardiac arrhythmia, cardiac hypertrophy, hypertension, cell proliferative disorders and diabetes.

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