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(2S, 4R)-Boc-4-aMino Pyrrolidine-2-carboxylate acid ethylester-HCl is a chemical compound utilized in organic synthesis and pharmaceutical research. It is an ester derivative of pyrrolidine-2-carboxylic acid, featuring a Boc-protected amino group at the 4 position. The HCl salt form is favored for its enhanced stability and solubility, making it a versatile component in the development of pharmaceuticals and agrochemicals, as well as in the study of enzyme mechanisms and peptide chemistry.

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  • (2S, 4R)-Boc-4-amino Pyrrolidine-2-carboxylate acid ethylester-HCl

    Cas No: 871014-58-3

  • USD $ 1.9-2.9 / Gram

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  • 871014-58-3 Structure
  • Basic information

    1. Product Name: (2S, 4R)-Boc-4-aMino Pyrrolidine-2-carboxylate acid ethylester-HCl
    2. Synonyms: (2S, 4R)-Boc-4-aMino Pyrrolidine-2-carboxylate acid ethylester-HCl;(2S,4R)-1-BOC-4-aMino Pyrrolidine-2-carboxylic acid ethylester-HCl;(2S,4R)-4-AMino-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid ethyl ester;(2S,4R)-1-tert-Butyl 2-ethyl 4-aMinopyrrolidine-1,2-dicarboxylate;(2S,4R)-4-amino-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxy;1,2-Pyrrolidinedicarboxylic acid, 4-amino-, 1-(1,1-dimethylethyl) 2-ethyl ester, (2S,4R)-;(2S,4R)-1-tert-Butyl 2-ethyl 4-aminopyrrolidine-1,2-dicarboxylate hydrochloride
    3. CAS NO:871014-58-3
    4. Molecular Formula: C12H22N2O4
    5. Molecular Weight: 258.31408
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 871014-58-3.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: (2S, 4R)-Boc-4-aMino Pyrrolidine-2-carboxylate acid ethylester-HCl(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2S, 4R)-Boc-4-aMino Pyrrolidine-2-carboxylate acid ethylester-HCl(871014-58-3)
    11. EPA Substance Registry System: (2S, 4R)-Boc-4-aMino Pyrrolidine-2-carboxylate acid ethylester-HCl(871014-58-3)
  • 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: 871014-58-3(Hazardous Substances Data)

871014-58-3 Usage

Uses

Used in Pharmaceutical Research and Development:
(2S, 4R)-Boc-4-aMino Pyrrolidine-2-carboxylate acid ethylester-HCl is used as a key intermediate in the synthesis of various pharmaceuticals. Its Boc-protected amino group allows for selective reactions and the formation of complex molecular structures, which are crucial for the development of new drugs with specific therapeutic properties.
Used in Agrochemical Synthesis:
In the agrochemical industry, (2S, 4R)-Boc-4-aMino Pyrrolidine-2-carboxylate acid ethylester-HCl is employed as a building block for the creation of novel agrochemicals. Its unique structure contributes to the development of pesticides, herbicides, and other agricultural chemicals that can improve crop yield and protect plants from pests and diseases.
Used in Enzyme Mechanism Studies:
(2S, 4R)-Boc-4-aMino Pyrrolidine-2-carboxylate acid ethylester-HCl is utilized as a substrate or inhibitor in the study of enzyme mechanisms. Its specific structure allows researchers to probe the catalytic activity and selectivity of enzymes, providing insights into their function and potential applications in biotechnology and medicine.
Used in Peptide Chemistry Research:
In the field of peptide chemistry, (2S, 4R)-Boc-4-aMino Pyrrolidine-2-carboxylate acid ethylester-HCl is used as a component in the synthesis of peptides and peptidomimetics. Its Boc protection strategy facilitates the stepwise assembly of peptide chains, enabling the production of bioactive peptides with potential applications in drug discovery and therapeutics.
Overall, (2S, 4R)-Boc-4-aMino Pyrrolidine-2-carboxylate acid ethylester-HCl is a valuable compound in the fields of pharmaceuticals, agrochemicals, enzyme research, and peptide chemistry, owing to its unique structure and properties that facilitate the development of innovative products and enhance our understanding of biological processes.

Check Digit Verification of cas no

The CAS Registry Mumber 871014-58-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,1,0,1 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 871014-58:
(8*8)+(7*7)+(6*1)+(5*0)+(4*1)+(3*4)+(2*5)+(1*8)=153
153 % 10 = 3
So 871014-58-3 is a valid CAS Registry Number.

871014-58-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Ethyl 1-(2-methyl-2-propanyl) (2S,4R)-4-amino-1,2-pyrrolidinedi carboxylate

1.2 Other means of identification

Product number -
Other names (2S, 4R)-4-AMINO-1-[T-BUTOXYCARBONYL]PYRROLIDINE-2-ETHYLCARBOXYLATE

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:871014-58-3 SDS

871014-58-3Downstream Products

871014-58-3Relevant articles and documents

HYDROGEN CHLORIDE SALT OF A SUBSTITUTED 5-OXAZOL-2-YL-QUINOLINE COMPOUND AND A PROCESS FOR THE PRODUCTION THEREOF

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Page/Page column 5, (2011/01/12)

The present invention relates to the compound of the Formula I: and to methods of treating upper and lower obstructive airway diseases using said compound, to formulations comprising it, and to a particular crystalline form and processes of synthesis of the crystalline form. IM=105109

XINAFOATE SALT OF A SUBSTITUTED 5-OXAZOL-2-YL-QUINOLINE COMPOUND

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Page/Page column 15; 17, (2008/06/13)

The present invention relates to the compound of the formula (I). To methods of treating upper and lower obstructive airway diseases using said compound, to formulations comprising it, and to polymorphs and processes of synthesis of the polymorphic forms.

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