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cis-5-AMino-2-Boc-hexahydro-cyclopenta[c]pyrrole is a chemical compound with a distinctive structure, derived from hexahydro-cyclopenta[c]pyrrole. It features an amino group and a Boc (tert-butoxycarbonyl) protecting group, which is commonly used to shield amine groups during organic synthesis. cis-5-AMino-2-Boc-hexahydro-cyclopenta[c]pyrrole holds promise in pharmaceutical research and organic chemistry as a building block for synthesizing more complex molecules. Its unique properties and reactivity make it a valuable asset in the development of innovative drugs and materials.

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  • 863600-81-1 Structure
  • Basic information

    1. Product Name: cis-5-AMino-2-Boc-hexahydro-cyclopenta[c]pyrrole
    2. Synonyms: cis-5-AMino-2-Boc-hexahydro-cyclopenta[c]pyrrole;endo-5-Amino-cis-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid tert-butyl ester
    3. CAS NO:863600-81-1
    4. Molecular Formula: C12H22N2O2
    5. Molecular Weight: 224.2994
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 863600-81-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: cis-5-AMino-2-Boc-hexahydro-cyclopenta[c]pyrrole(CAS DataBase Reference)
    10. NIST Chemistry Reference: cis-5-AMino-2-Boc-hexahydro-cyclopenta[c]pyrrole(863600-81-1)
    11. EPA Substance Registry System: cis-5-AMino-2-Boc-hexahydro-cyclopenta[c]pyrrole(863600-81-1)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 863600-81-1(Hazardous Substances Data)

863600-81-1 Usage

Uses

Used in Pharmaceutical Research:
cis-5-AMino-2-Boc-hexahydro-cyclopenta[c]pyrrole is utilized as a key intermediate in the synthesis of pharmaceutical compounds. Its unique structure and reactivity allow for the creation of new drug candidates with potential therapeutic applications.
Used in Organic Chemistry:
In the field of organic chemistry, cis-5-AMino-2-Boc-hexahydro-cyclopenta[c]pyrrole serves as a building block for the assembly of more complex organic molecules. Its presence enables chemists to explore novel synthetic pathways and develop advanced materials with specific properties.
Used in Drug Development:
cis-5-AMino-2-Boc-hexahydro-cyclopenta[c]pyrrole is employed as a precursor in drug development, where its unique structure can be leveraged to create new pharmaceutical agents. Its potential applications in this area highlight its importance in the advancement of medicinal chemistry.
Used in Material Science:
cis-5-AMino-2-Boc-hexahydro-cyclopenta[c]pyrrole also finds use in material science, where its properties can be harnessed to develop new materials with specific characteristics. This can include the creation of novel polymers, coatings, or other materials with tailored properties for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 863600-81-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,3,6,0 and 0 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 863600-81:
(8*8)+(7*6)+(6*3)+(5*6)+(4*0)+(3*0)+(2*8)+(1*1)=171
171 % 10 = 1
So 863600-81-1 is a valid CAS Registry Number.

863600-81-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Meso-(3aR,5r,6aS)-tert-butyl 5-aminohexahydrocyclopenta[c]pyrrole-2(1H)-carboxylate

1.2 Other means of identification

Product number -
Other names -

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:863600-81-1 SDS

863600-81-1Relevant articles and documents

DIHYDROPTERIDINONE DERIVATIVES, PREPARATION PROCESS AND PHARMACEUTICAL USE THEREOF

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Page/Page column 31, (2012/08/08)

Dihydroperidinone derivatives, preparation process and pharmaceutical use thereof are disclosed. Specially, new dihydroperidinone derivatives represented by general formula (I), wherein each substituent of the general formula (I) is defined as in the description, their preparation process, pharmaceutical compositions comprising said derivatives and their use as therapeutical agents, especially as Plk kinase inhibitors are disclosed.

DIHYDROPTERIDINONE DERIVATIVES, PREPARATION PROCESS AND PHARMACEUTICAL USE THEREOF

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Page/Page column 34, (2012/07/28)

Dihydroperidinone derivatives, preparation process and pharmaceutical use thereof are disclosed. Specially, new dihydroperidinone derivatives represented by general formula (I), wherein each substituent of the general formula (I) is defined as in the description, their preparation process, pharmaceutical compositions comprising said derivatives and their use as therapeutical agents, especially as Plk kinase inhibitors are disclosed.

Evaluation of a 3-amino-8-azabicyclo[3.2.1]octane replacement in the CCR5 antagonist maraviroc

Lemoine, Rémy C.,Petersen, Ann C.,Setti, Lina,Baldinger, Thomas,Wanner, Jutta,Jekle, Andreas,Heilek, Gabrielle,deRosier, André,Ji, Changhua,Rotstein, David M.

scheme or table, p. 1674 - 1676 (2010/07/03)

The bicyclic 5-amino-3-azabicyclo[3.3.0]octanes were shown to be effective replacements for the 3-amino-8-azabicyclo[3.2.1]octane found in the CCR5 antagonist maraviroc.

An octahydro-cyclopenta[c]pyrrole series of inhibitors of the type 1 glycine transporter

Lowe III, John A.,DeNinno, Shari L.,Drozda, Susan E.,Schmidt, Christopher J.,Ward, Karen M.,David Tingley III,Sanner, Mark,Tunucci, Don,Valentine, James

supporting information; experimental part, p. 907 - 911 (2010/08/19)

We describe a novel series of inhibitors of the type 1 glycine transporter (GlyT1) as an approach to relieving the glutamatergic deficit that is thought to underlie schizophrenia. Synthesis and SAR follow-up of a series of octahydro-cyclopenta[c]pyrrole derivatives afforded potent in vitro inhibition of GlyT1 as well as in vivo activity in elevating CSF glycine. We also found that a 3-O(c-pentyl), 4-F substituent may serve as a surrogate for the widely used 3-trifluoromethoxy group, suggesting its application as an isostere for future medicinal chemistry studies.

Substituted bicycloalkylamine derivatives as modulators of chemokine receptor activity

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Page/Page column 19, (2010/02/14)

The present application describes modulators of MCP-1 of formula (I): or stereoisomers or pharmaceutically acceptable salts thereof, wherein X, Z, a, b, c, d, n, R1, R2, R3, R4, R5, R10, R

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