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100119-45-7

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100119-45-7 Usage

General Description

4-phenyltetrahydropyran-4-carbonyl chloride is a chemical compound with the molecular formula C14H15ClO2. It is derived from tetrahydropyran, a six-membered heterocyclic compound, and contains a carbonyl chloride functional group at the 4-position of the tetrahydropyran ring. 4-phenyltetrahydropyran-4-carbonyl chloride is most commonly used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It can undergo various chemical reactions, such as acyl substitution and nucleophilic addition, to form a wide range of other organic compounds. Due to its versatile reactivity and utility in chemical synthesis, 4-phenyltetrahydropyran-4-carbonyl chloride is a valuable compound in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 100119-45-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,1,1 and 9 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 100119-45:
(8*1)+(7*0)+(6*0)+(5*1)+(4*1)+(3*9)+(2*4)+(1*5)=57
57 % 10 = 7
So 100119-45-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H13ClO2/c13-11(14)12(6-8-15-9-7-12)10-4-2-1-3-5-10/h1-5H,6-9H2

100119-45-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-phenyloxane-4-carbonyl chloride

1.2 Other means of identification

Product number -
Other names F2190-0168

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:100119-45-7 SDS

100119-45-7Relevant articles and documents

Achiral Derivatives of Hydroxamate AR-42 Potently Inhibit Class i HDAC Enzymes and Cancer Cell Proliferation

Tng, Jiahui,Lim, Junxian,Wu, Kai-Chen,Lucke, Andrew J.,Xu, Weijun,Reid, Robert C.,Fairlie, David P.

supporting information, p. 5956 - 5971 (2020/06/05)

AR-42 is an orally active inhibitor of histone deacetylases (HDACs) in clinical trials for multiple myeloma, leukemia, and lymphoma. It has few hydrogen bond donors and acceptors but is a chiral 2-arylbutyrate and potentially prone to racemization. We report achiral AR-42 analogues incorporating a cycloalkyl group linked via a quaternary carbon atom, with up to 40-fold increased potency against human class I HDACs (e.g., JT86, IC50 0.7 nM, HDAC1), 25-fold increased cytotoxicity against five human cancer cell lines, and up to 70-fold less toxicity in normal human cells. JT86 was ninefold more potent than racAR-42 in promoting accumulation of acetylated histone H4 in MM96L melanoma cells. Molecular modeling and structure-activity relationships support binding to HDAC1 with tetrahydropyran acting as a hydrophobic shield from water at the enzyme surface. Such potent inhibitors of class I HDACs may show benefits in diseases (cancers, parasitic infections, inflammatory conditions) where AR-42 is active.

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