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39503-58-7

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39503-58-7 Usage

Description

METHYL 5-BROMO-2-METHOXY-4-METHYLBENZOATE is a chemical compound belonging to the class of benzoate esters. It is a white to off-white crystalline solid with a molecular formula C10H11BrO3 and a molecular weight of 263.09 g/mol.
Used in Pharmaceutical Industry:
METHYL 5-BROMO-2-METHOXY-4-METHYLBENZOATE is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of various organic compounds.
Used in Agrochemical Production:
METHYL 5-BROMO-2-METHOXY-4-METHYLBENZOATE is used in the production of agrochemicals, where it plays a role in the creation of substances that help in the management and protection of crops.
Used in Fragrance Industry:
METHYL 5-BROMO-2-METHOXY-4-METHYLBENZOATE is used as a component in the fragrance industry, contributing to the formulation of various scented products.
Used in Specialty Chemicals Production:
METHYL 5-BROMO-2-METHOXY-4-METHYLBENZOATE is utilized in the production of specialty chemicals, which are important for a range of applications across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 39503-58-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,5,0 and 3 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 39503-58:
(7*3)+(6*9)+(5*5)+(4*0)+(3*3)+(2*5)+(1*8)=127
127 % 10 = 7
So 39503-58-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H11BrO3/c1-6-4-9(13-2)7(5-8(6)11)10(12)14-3/h4-5H,1-3H3

39503-58-7Relevant articles and documents

HSP90B N-TERMINAL ISOFORM-SELECTIVE INHIBITORS

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Paragraph 0109; 0110; 0170; 0171, (2018/08/03)

The present technology provides compounds according to Formula (I) as well as compositions including such compounds useful for the treatment of cancers such as non-small cell lung cancer, bladder cancer, or colon cancer.

Rational approach to highly potent and selective apoptosis signal-regulating kinase 1 (ASK1) inhibitors

Lovering, Frank,Morgan, Paul,Allais, Christophe,Aulabaugh, Ann,Brodfuehrer, Joanne,Chang, Jeanne,Coe, Jotham,Ding, WeiDong,Dowty, Heather,Fleming, Margaret,Frisbie, Richard,Guzova, Julia,Hepworth, David,Jasti, Jayasankar,Kortum, Steve,Kurumbail, Ravi,Mohan, Shashi,Papaioannou, Nikolaos,Strohbach, Joseph W.,Vincent, Fabien,Lee, Katherine,Zapf, Christoph W.

, p. 606 - 621 (2018/01/19)

Many diseases are believed to be driven by pathological levels of reactive oxygen species (ROS) and oxidative stress has long been recognized as a driver for inflammatory disorders. Apoptosis signal-regulating kinase 1 (ASK1) has been reported to be activ

Improved replicon cellular activity of non-nucleoside allosteric inhibitors of HCV NS5B polymerase: From benzimidazole to indole scaffolds

Beaulieu, Pierre L.,Gillard, James,Bykowski, Darren,Brochu, Christian,Dansereau, Nathalie,Duceppe, Jean-Simon,Hache, Bruno,Jakalian, Araz,Lagace, Lisette,LaPlante, Steven,McKercher, Ginette,Moreau, Elaine,Perreault, Stephane,Stammers, Timothy,Thauvette, Louise,Warrington, Jeff,Kukolj, George

, p. 4987 - 4993 (2007/10/03)

Benzimidazole-based allosteric inhibitors of the hepatitis C virus (HCV) NS5B polymerase were diversified to a variety of topologically related scaffolds. Replacement of the polar benzimidazole core by lipophilic indoles led to inhibitors with improved potency in the cell-based subgenomic HCV replicon system. Transposing the indole scaffold into a previously described series of benzimidazole-tryptophan amides generated the most potent inhibitors of HCV RNA replication in cell culture reported to date in this series (EC50 ~ 50 nM).

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