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Methyl 6,6-difluorobicyclo[3.1.0]hexane-3-carboxylate is a heterocyclic compound with a bicyclic structure that features a unique fluorinated cyclopropane ring. As a carboxylate ester, it possesses a carboxylic acid functional group attached to an aliphatic chain. This distinctive structure and chemical properties make it a promising candidate for applications in organic synthesis and medicinal chemistry.

1093750-99-2

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1093750-99-2 Usage

Uses

Used in Organic Synthesis:
Methyl 6,6-difluorobicyclo[3.1.0]hexane-3-carboxylate serves as a valuable building block in the synthesis of complex organic molecules. Its unique structure allows for the creation of a variety of compounds with potential applications across different industries.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, methyl 6,6-difluorobicyclo[3.1.0]hexane-3-carboxylate is utilized as a key intermediate in the development of pharmaceuticals. Its distinctive fluorinated cyclopropane ring can contribute to the design of novel drugs with improved properties, such as enhanced potency, selectivity, and bioavailability.
Used in Drug Discovery and Development:
Researchers in drug discovery and development find methyl 6,6-difluorobicyclo[3.1.0]hexane-3-carboxylate to be a valuable tool. Its incorporation into the molecular structures of potential drugs can lead to the discovery of new therapeutic agents with unique mechanisms of action and the potential to treat a wide range of diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 1093750-99-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,3,7,5 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1093750-99:
(9*1)+(8*0)+(7*9)+(6*3)+(5*7)+(4*5)+(3*0)+(2*9)+(1*9)=172
172 % 10 = 2
So 1093750-99-2 is a valid CAS Registry Number.

1093750-99-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 6,6-difluorobicyclo[3.1.0]hexane-3-carboxylate

1.2 Other means of identification

Product number -
Other names methyl 6,6-difluorobicyclo[3.1.0]hexane-3-carboxylate

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:1093750-99-2 SDS

1093750-99-2Relevant academic research and scientific papers

Synthesis of Functionalized Difluorocyclopropanes: Unique Building Blocks for Drug Discovery

Bychek, Roman M.,Levterov, Vadym V.,Sadkova, Iryna V.,Tolmachev, Andrey A.,Mykhailiuk, Pavel K.

supporting information, p. 12291 - 12297 (2018/03/28)

Difluorocyclopropane-containing building blocks for drug discovery were synthesized from the functionalized alkenes and TMSCF3/NaI. Novel fluorinated acids, amines, amino acids, alcohols, ketones and sulfonyl chlorides were obtained.

COMBINATIONS OF HEPATITIS C VIRUS INHIBITORS

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Page/Page column 515; 516, (2015/02/02)

The present disclosure is generally directed to antiviral compounds, and more specifically directed to combinations of compounds which can inhibit the function of the NS5A protein encoded by Hepatitis C virus (HCV), compositions comprising such combinations, and methods for inhibiting the function of the NS5A protein.

SUBSTITUTED ARYL PYRIMIDINONE DERIVATIVES

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Page/Page column 46-47, (2009/10/22)

Substituted aryl pyrimidinone derivatives are provided, of the Formula: wherein variables are as described herein. Such compounds are ligands that may be used to modulate specific receptor activity in vivo or in vitro, and are particularly useful in the treatment of conditions associated with pathological receptor activation in humans, domesticated companion animals and livestock animals. Pharmaceutical compositions and methods for using such compounds to treat such disorders are provided, as are methods for using such ligands for receptor localization studies.

SUBSTITUTED ARYL PYRIMIDINONES

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Page/Page column 48, (2009/10/09)

Substituted aryl pyrimidinones are provided, of the Formula (I) wherein variables are as described herein. Such compounds are ligands that may be used to modulate specific receptor activity in vivo or in vitro, and are particularly useful in the treatment of conditions associated with pathological receptor activation in humans, domesticated companion animals and livestock animals. Pharmaceutical compositions and methods for using such compounds to treat such disorders are provided, as are methods for using such ligands for receptor localization studies.

SUBSTITUTED PYRIMIDINONES

-

Page/Page column 64, (2009/01/23)

Substituted pyrimidinones are provided, of the Formula (I): wherein variables are as described herein. Such compounds are ligands that may be used to modulate specific receptor activity in vivo or in vitro, and are particularly useful in the treatment of conditions associated with pathological receptor activation in humans, domesticated companion animals and livestock animals. Pharmaceutical compositions and methods for using such compounds to treat such disorders are provided, as are methods for using such ligands for receptor localization studies.

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