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180322-86-5

(1R,2R)-N-BOC-1-AMINO-2-PHENYLCYCLOPROPANECARBOXYLIC ACID is a chiral amino acid derivative featuring a cyclopropane ring, a carboxylic acid group, and an N-BOC (tert-butyloxycarbonyl) protected amino group. (1R,2R)-N-BOC-1-AMINO-2-PHENYLCYCLOPROPANECARBOXYLIC ACID is of interest to synthetic and medicinal chemists due to its unique structure and functional groups, and it holds potential for applications in organic synthesis and the development of bioactive molecules.

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  • 180322-86-5 Structure

  • Basic information

    1. Product Name: (1R,2R)-N-BOC-1-AMINO-2-PHENYLCYCLOPROPANECARBOXYLIC ACID
    2. Synonyms: (1R,2R)-N-BOC-1-AMINO-2-PHENYLCYCLOPROPANECARBOXYLIC ACID;(1R,2R)-C-1-(BOC-AMINO)-2-PHENYLCYCLOPRO PANECARBOXYLIC ACID;(1R,2R)-cis-1-(Boc-amino)-2-phenylcyclopropanecarboxylic acid;(1R,2R)-N-BOC-1-AMINO-2-PHENYLCYCLOPROPANECARBOXYLIC ACID(WX160312)
    3. CAS NO:180322-86-5
    4. Molecular Formula: C15H19NO4
    5. Molecular Weight: 277.32
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 180322-86-5.mol

  • Chemical Properties

    1. Melting Point: 180-182 °C
    2. Boiling Point: 420.18°C (rough estimate)
    3. Flash Point: 226.1°C
    4. Appearance: /
    5. Density: 1.1311 (rough estimate)
    6. Vapor Pressure: 6.78E-09mmHg at 25°C
    7. Refractive Index: 1.5080 (estimate)
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (1R,2R)-N-BOC-1-AMINO-2-PHENYLCYCLOPROPANECARBOXYLIC ACID(CAS DataBase Reference)
    11. NIST Chemistry Reference: (1R,2R)-N-BOC-1-AMINO-2-PHENYLCYCLOPROPANECARBOXYLIC ACID(180322-86-5)
    12. EPA Substance Registry System: (1R,2R)-N-BOC-1-AMINO-2-PHENYLCYCLOPROPANECARBOXYLIC ACID(180322-86-5)

  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 36/37/38
    3. Safety Statements: 37/39-26
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 180322-86-5(Hazardous Substances Data)

180322-86-5 Usage

Uses

Used in Organic Synthesis:
(1R,2R)-N-BOC-1-AMINO-2-PHENYLCYCLOPROPANECARBOXYLIC ACID is used as a key intermediate in the synthesis of complex organic molecules, particularly in the creation of peptidomimetics and other bioactive compounds. Its unique cyclopropane ring and protected amino group facilitate the development of novel chemical entities with potential applications in various fields.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (1R,2R)-N-BOC-1-AMINO-2-PHENYLCYCLOPROPANECARBOXYLIC ACID is utilized as a building block for the design and synthesis of new drugs. Ongoing studies are exploring its biological activity and potential as a therapeutic agent, with the aim of discovering its effects on various biological targets and its suitability for treating specific diseases.
Used in Medicinal Chemistry:
(1R,2R)-N-BOC-1-AMINO-2-PHENYLCYCLOPROPANECARBOXYLIC ACID is employed as a versatile component in medicinal chemistry for the development of innovative drug candidates. Its chiral center and functional groups allow for the fine-tuning of molecular properties, which can lead to the optimization of drug efficacy, selectivity, and pharmacokinetics.

Check Digit Verification of cas no

The CAS Registry Mumber 180322-86-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,0,3,2 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 180322-86:
(8*1)+(7*8)+(6*0)+(5*3)+(4*2)+(3*2)+(2*8)+(1*6)=115
115 % 10 = 5
So 180322-86-5 is a valid CAS Registry Number.
InChI:InChI=1/C15H19NO4/c1-14(2,3)20-13(19)16-15(12(17)18)9-11(15)10-7-5-4-6-8-10/h4-8,11H,9H2,1-3H3,(H,16,19)(H,17,18)/p-1/t11-,15-/m1/s1

180322-86-5SDS

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 (1R,2R)-N-BOC-1-AMINO-2-PHENYLCYCLOPROPANECARBOXYLIC ACID

1.2 Other means of identification

Product number -
Other names (1R,2R)-C-1-(BOC-AMINO)-2-PHENYLCYCLOPRO PANECARBOXYLIC ACID

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:180322-86-5 SDS

180322-86-5Relevant articles and documents

Asymmetric cyclopropanations by rhodium(II) N-(arylsulfonyl)prolinate catalyzed decomposition of vinyldiazomethanes in the presence of alkenes. Practical enantioselective synthesis of the four stereoisomers of 2-phenylcyclopropan-1-amino acid

Davies, Huw M. L.,Bruzinski, Paul R.,Lake, Debra H.,Kong, Norman,Fall, Michael J.

, p. 6897 - 6907 (2007/10/03)

The rhodium N-(arylsulfonyl)prolinate catalyzed decomposition of vinyldiazomethanes in the presence of alkenes leads to a very general method for the synthesis of functionalized cyclopropanes in a highly diastereoselective and enantioselective mode. A det

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