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188875-37-8

CarbaMic acid, [(2R)-2-amino-2-phenylethyl]-, 1,1-dimethylethyl ester, is a chemical compound with the molecular formula C13H21NO3. It is an ester of CarbaMic acid and is derived from the amino acid phenylalanine. CarbaMic acid, [(2R)-2-aMino-2-phenylethyl]-, 1,1-diMethylethyl ester has potential applications in various fields, including pharmaceuticals, organic synthesis, and biochemical and biomedical research.

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  • 188875-37-8 Structure

  • Basic information

    1. Product Name: CarbaMic acid, [(2R)-2-aMino-2-phenylethyl]-, 1,1-diMethylethyl ester
    2. Synonyms: CarbaMic acid, [(2R)-2-aMino-2-phenylethyl]-, 1,1-diMethylethyl ester;(R)-N2-Boc-1-phenylethylenediaMine;1,1-Dimethylethyl ((2R)-2-amino-2-phenylethyl)carbamate
    3. CAS NO:188875-37-8
    4. Molecular Formula: C13H20N2O2
    5. Molecular Weight: 236.3101
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 188875-37-8.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.: under inert gas (nitrogen or Argon) at 2–8 °C
    8. Solubility: N/A
    9. CAS DataBase Reference: CarbaMic acid, [(2R)-2-aMino-2-phenylethyl]-, 1,1-diMethylethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: CarbaMic acid, [(2R)-2-aMino-2-phenylethyl]-, 1,1-diMethylethyl ester(188875-37-8)
    11. EPA Substance Registry System: CarbaMic acid, [(2R)-2-aMino-2-phenylethyl]-, 1,1-diMethylethyl ester(188875-37-8)

  • 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: 188875-37-8(Hazardous Substances Data)

188875-37-8 Usage

Uses

Used in Pharmaceutical Industry:
CarbaMic acid, [(2R)-2-amino-2-phenylethyl]-, 1,1-dimethylethyl ester is used as a building block for the synthesis of various pharmaceuticals. Its unique structure and properties make it a valuable component in the development of new drugs and therapeutic agents.
Used in Organic Synthesis:
In the field of organic synthesis, CarbaMic acid, [(2R)-2-amino-2-phenylethyl]-, 1,1-dimethylethyl ester serves as an intermediate. Its reactivity and functional groups allow for further chemical modifications and the creation of more complex molecules.
Used in Biochemical and Biomedical Studies:
CarbaMic acid, [(2R)-2-amino-2-phenylethyl]-, 1,1-dimethylethyl ester is also used as a research chemical in biochemical and biomedical studies. Its potential interactions with biological systems and its ability to serve as a model compound for understanding certain biological processes make it a valuable tool for researchers in these fields.

Check Digit Verification of cas no

The CAS Registry Mumber 188875-37-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,8,7 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 188875-37:
(8*1)+(7*8)+(6*8)+(5*8)+(4*7)+(3*5)+(2*3)+(1*7)=208
208 % 10 = 8
So 188875-37-8 is a valid CAS Registry Number.

188875-37-8 Well-known Company Product Price

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  • Aldrich

  • (JWP00375)  (R)-(2-Amino-2-phenyl-ethyl)-carbamic acid tert-butyl ester  AldrichCPR

  • 188875-37-8

  • JWP00375-1G

  • 7,733.70CNY

  • Detail

188875-37-8SDS

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 Carbamic acid, N-?[(2R)?-?2-?amino-?2-?phenylethyl]?-?, 1,?1-?dimethylethyl ester

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 -
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More Details:188875-37-8 SDS

188875-37-8Relevant articles and documents

Enantioselective Strecker and Allylation Reactions with Aldimines Catalyzed by Chiral Oxazaborolidinium Ions

Kang, Ki-Tae,Park, Sang Hyun,Ryu, Do Hyun

, p. 6679 - 6683 (2019/09/12)

Chiral oxazaborolidinium ion (COBI)-catalyzed enantioselective nucleophilic addition reactions of aldimines using tributyltin cyanide and allyltributylstannane have been developed. Various α-aminonitriles and homoallylic amines were synthesized in high yi

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