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methyl (3-bromophenyl)glycinate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

126689-75-6

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126689-75-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126689-75-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,6,8 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 126689-75:
(8*1)+(7*2)+(6*6)+(5*6)+(4*8)+(3*9)+(2*7)+(1*5)=166
166 % 10 = 6
So 126689-75-6 is a valid CAS Registry Number.

126689-75-6Relevant academic research and scientific papers

Acid-catalyzed chemodivergent reactions of 2,2-dimethoxyacetaldehyde and anilines

Guo, Luxia,Chen, Zihao,Zhu, Hongmei,Li, Minghao,Gu, Yanlong

supporting information, p. 1419 - 1422 (2020/11/12)

Chemodivergent reactions of 2,2-dimethoxyacetaldehyde and anilines were described, which were established on the basis of either a C[sbnd]C bond cleavage or a rearrangement process of a reaction intermediate. These reactions proceeded in a condition-determined manner with good functional group tolerance. In the first model, 2,2-dimethoxyacetaldehyde reacted with aniline to form a new C[sbnd]N bond, in the presence of O2, via a C[sbnd]C bond cleavage reaction. However, in the second model, by performing the reaction in the absence of O2, Heyns rearrangement occurred and generated a new C[sbnd]O bond to form methyl phenylglycinate. Such condition-determined reactions not only offered the new way for value-added conversion of biomass-derived platform molecule, 2, 2-dimethoxyacetaldehyde, but also provided efficient methods for the synthesis of N-arylformamides and methyl phenylglycinates.

Structure-based design of protein tyrosine phosphatase-1B inhibitors

Black, Emma,Breed, Jason,Breeze, Alexander L.,Embrey, Kevin,Garcia, Robert,Gero, Thomas W.,Godfrey, Linda,Kenny, Peter W.,Morley, Andrew D.,Minshull, Claire A.,Pannifer, Andrew D.,Read, Jon,Rees, Amanda,Russell, Daniel J.,Toader, Dorin,Tucker, Julie

, p. 2503 - 2507 (2007/10/03)

Using structure-based design, a new class of inhibitors of protein tyrosine phosphatase-1B (PTP1B) has been identified, which incorporate the 1,2,5-thiadiazolidin-3-one-1,1-dioxide template.

5- (SUBSTITUTED PHENYL) -THIADIAZOLIDINE-3-ONES AND THEIR USE AS PTP1B

-

Page 62, (2010/02/07)

The invention concerns compounds of the formula (I) or pharmaceutically acceptable salts thereof (A chemical formula should be inserted here - please see paper copy enclosed herewith) wherein R1, R2, R3, R4, R5, and R6 have any of the meanings defined in the description. Processes for the manufacture of compounds of formula (I), compositions containing them, their use as inhibitors of protein tyrosine phosphatase PTP1B and their use for the treatment of diabetes mellitus are also described.

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