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1-(tert-butoxycarbonyl)-4,4-difluoropyrrolidine-2-carboxylic acid is a chemical compound characterized by its five-membered heterocyclic pyrrolidine ring, with a tert-butoxycarbonyl (Boc) protecting group and two fluorine atoms. 1-(tert-butoxycarbonyl)-4,4-difluoropyrrolidine-2-carboxylic acid is utilized in the pharmaceutical industry for the synthesis of various drugs, offering a unique combination of structural features that can enhance the pharmacokinetic properties of the resulting medications.
Used in Pharmaceutical Industry:
1-(tert-butoxycarbonyl)-4,4-difluoropyrrolidine-2-carboxylic acid is used as a synthetic intermediate for the development of pharmaceuticals due to its ability to be incorporated into complex organic molecules. The presence of the Boc group serves to protect amines during organic synthesis, while the fluorine atoms can improve the pharmacokinetic profile of the drugs, potentially leading to better absorption, distribution, metabolism, and excretion.
1-(tert-butoxycarbonyl)-4,4-difluoropyrrolidine-2-carboxylic acid is also used as a building block in medicinal chemistry research for the creation of more complex organic molecules. Its precise synthesis and properties make it a valuable tool in the design and synthesis of new pharmaceutical agents, contributing to the advancement of drug discovery and development processes.

1000313-01-8

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1000313-01-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1000313-01-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,0,3,1 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1000313-01:
(9*1)+(8*0)+(7*0)+(6*0)+(5*3)+(4*1)+(3*3)+(2*0)+(1*1)=38
38 % 10 = 8
So 1000313-01-8 is a valid CAS Registry Number.

1000313-01-8SDS

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 4,4-difluoro-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidine-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names HT1190

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:1000313-01-8 SDS

1000313-01-8Downstream Products

1000313-01-8Relevant academic research and scientific papers

FUSED MORPHOLINOPYRIMIDINES AND METHODS OF USE THEREOF

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Paragraph 1795, (2017/05/14)

The present disclosure relates to Fused Morpholinopyrimidines, pharmaceutical compositions comprising an effective amount of a Fused Morpholinopyrimidine and methods for using a Fused Morpholinopyrimidine in the treatment of a neurodegenerative disease, comprising administering to a subject in need thereof an effective amount of a Fused Morpholinopyrimidine.

FUSED MORPHOLINOPYRIMIDINES AND METHODS OF USE THEREOF

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Paragraph 1231, (2015/08/03)

The present disclosure relates to Fused Morpholinopyrimidines, pharmaceutical compositions comprising an effective amount of a Fused Morpholinopyrimidine and methods for using a Fused Morpholinopyrimidine in the treatment of a neurodegenerative disease, comprising administering to a subject in need thereof an effective amount of a Fused Morpholinopyrimidine.

METABOTROPIC GLUTAMATE RECEPTOR 5 MODULATORS AND METHODS OF USE THEREOF

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, (2013/02/27)

Compounds that modulate GluR5 activity and methods of using the same are disclosed.

PYRRO[1,2-B]PYRIDAZINONE COMPOUNDS

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, (2008/06/13)

The invention is directed to pyrro[l,2-b]pyridazinone compounds and pharmaceutical compositions containing such compounds that are useful in treating infections by hepatitis C virus.

VLA-4 inhibitor compounds

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, (2008/06/13)

Compounds that selectively inhibit the binding of ligands to alpha4beta1 integrin (VLA-4) and methods for their preparation are disclosed. In one embodiment, compounds of the invention are represented by Formula I: As selective inhibitors of VLA-4 mediated cell adhesion, compounds of the present invention are useful in the treatment of conditions associated with such adhesion, including, but not limited to, such conditions as inflammatory and autoimmune responses, diabetes, asthma, psoriasis, inflammatory bowel disease, transplantation rejection, and tumor metastasis. Also disclosed are pharmaceutical compositions, methods of inhibiting VLA-4 mediated cell adhesion and methods of treating conditions associated with LA-4 mediated cell adhesion, which involve compounds of Formula I.

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