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1227576-36-4

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1227576-36-4 Usage

Description

(6-Bromo-2-methyl-pyridin-3-yl)-methanol is a chemical compound characterized by its molecular formula C7H8BrNO. It features a bromine atom, a methyl group, a pyridine ring, and a hydroxyl group. (6-Bromo-2-methyl-pyridin-3-yl)-methanol is recognized for its potential in organic synthesis and pharmaceutical research, where it serves as a key building block for creating a variety of biologically active molecules. Its unique structural attributes and functional groups have positioned (6-Bromo-2-methyl-pyridin-3-yl)-methanol as a significant asset in medicinal chemistry and the ongoing quest for novel drug discoveries.

Uses

Used in Pharmaceutical Research:
(6-Bromo-2-methyl-pyridin-3-yl)-methanol is used as a synthetic building block for the development of biologically active compounds. Its unique structure and functional groups contribute to the creation of new pharmaceutical agents with potential medicinal properties.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (6-Bromo-2-methyl-pyridin-3-yl)-methanol is utilized as a valuable tool for the synthesis of diverse drug candidates. Its structural features and reactivity make it a promising starting point for designing and optimizing new therapeutic molecules.
Used in Drug Discovery:
(6-Bromo-2-methyl-pyridin-3-yl)-methanol is employed as a key component in drug discovery processes. Its incorporation into various chemical libraries aids researchers in identifying and developing new drugs with improved efficacy and selectivity.
Used in Organic Synthesis:
(6-Bromo-2-methyl-pyridin-3-yl)-methanol is used as a versatile intermediate in organic synthesis, allowing for the creation of a wide range of chemical products with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 1227576-36-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,7,5,7 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1227576-36:
(9*1)+(8*2)+(7*2)+(6*7)+(5*5)+(4*7)+(3*6)+(2*3)+(1*6)=164
164 % 10 = 4
So 1227576-36-4 is a valid CAS Registry Number.

1227576-36-4Downstream Products

1227576-36-4Relevant articles and documents

PYRIDYLPYRIDONE DERIVATIVE USEFUL AS A RET KINASE INHIBITOR IN THE TREATMENT OF IBS AND CANCER

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, (2017/09/09)

This invention relates to a novel compound which is an inhibitor of the Rearranged during Transfection (RET) kinase, to pharmaceutical compositions containing it, to processes for its preparation, and to its use in therapy, alone or in combination, for the normalization of gastrointestinal sensitivity, motility and/or secretion and/or abdominal disorders or diseases and/or treatment related to diseases related to RET dysfunction or where modulation of RET activity may have therapeutic benefit including but not limited to all classifications of irritable bowel syndrome (IBS) including diarrhea-predominant, constipation-predominant or alternating stool pattern, functional bloating, functional constipation, functional diarrhea, unspecified functional bowel disorder, functional abdominal pain syndrome, chronic idiopathic constipation, functional esophageal disorders, functional gastroduodenal disorders, functional anorectal pain, inflammatory bowel disease, proliferative diseases such as non-small cell lung cancer, hepatocellular carcinoma, colorectal cancer, medullary thyroid cancer, follicular thyroid cancer, anaplastic thyroid cancer, papillary thyroid cancer, brain tumors, peritoneal cavity cancer, solid tumors, other lung cancer, head and neck cancer, gliomas, neuroblastomas, Von Hippel-Lindau Syndrome and kidney tumors, breast cancer, fallopian tube cancer, ovarian cancer, transitional cell cancer, prostate cancer, cancer of the esophagus and gastroesophageal junction, biliary cancer, adenocarcinoma, and any malignancy with increased RET kinase activity. Formula (I)

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