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4-(2-Tert-butoxycarbonylamino-3-phenyl-propionylamino)-butyric acid is a complex organic compound with the molecular formula C18H26N2O5. It is a derivative of butyric acid, featuring a 3-phenyl-propionylamino group and a 2-tert-butoxycarbonylamino group attached to the 4-position of the butyric acid backbone. 4-(2-TERT-BUTOXYCARBONYLAMINO-3-PHENYL-PROPIONYLAMINO)-BUTYRIC ACID is of interest in the field of organic chemistry and may have potential applications in the synthesis of pharmaceuticals or other chemical products due to its unique structure and functional groups.

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  • 4-(2-TERT-BUTOXYCARBONYLAMINO-3-PHENYL-PROPIONYLAMINO)-BUTYRIC ACID

    Cas No: 112670-47-0

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  • 112670-47-0 Structure
  • Basic information

    1. Product Name: 4-(2-TERT-BUTOXYCARBONYLAMINO-3-PHENYL-PROPIONYLAMINO)-BUTYRIC ACID
    2. Synonyms: 4-(2-((tert-Butoxycarbonyl)aMino)-3-phenylpropanaMido)butanoic acid
    3. CAS NO:112670-47-0
    4. Molecular Formula: C18H26N2O5
    5. Molecular Weight: 350.41
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 112670-47-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 614°Cat760mmHg
    3. Flash Point: 325.1°C
    4. Appearance: /
    5. Density: 1.165g/cm3
    6. Vapor Pressure: 6.25E-16mmHg at 25°C
    7. Refractive Index: N/A
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 4-(2-TERT-BUTOXYCARBONYLAMINO-3-PHENYL-PROPIONYLAMINO)-BUTYRIC ACID(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-(2-TERT-BUTOXYCARBONYLAMINO-3-PHENYL-PROPIONYLAMINO)-BUTYRIC ACID(112670-47-0)
    12. EPA Substance Registry System: 4-(2-TERT-BUTOXYCARBONYLAMINO-3-PHENYL-PROPIONYLAMINO)-BUTYRIC ACID(112670-47-0)
  • 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: 112670-47-0(Hazardous Substances Data)

112670-47-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112670-47-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,6,7 and 0 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 112670-47:
(8*1)+(7*1)+(6*2)+(5*6)+(4*7)+(3*0)+(2*4)+(1*7)=100
100 % 10 = 0
So 112670-47-0 is a valid CAS Registry Number.
InChI:InChI=1/C18H26N2O5/c1-18(2,3)25-17(24)20-14(12-13-8-5-4-6-9-13)16(23)19-11-7-10-15(21)22/h4-6,8-9,14H,7,10-12H2,1-3H3,(H,19,23)(H,20,24)(H,21,22)/p-1/t14-/m1/s1

112670-47-0SDS

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 4-[[2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-phenylpropanoyl]amino]butanoic acid

1.2 Other means of identification

Product number -
Other names 4-(2-tert-Butoxycarbonylamino-3-phenyl-propionylamino)-butyric 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:112670-47-0 SDS

112670-47-0Relevant articles and documents

Prodrugs of compounds that enhance antifungal activity and compositions of said prodrugs

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Page/Page column 65; 66; 67; 74, (2017/05/17)

The invention relates to prodrugs for use in the inhibition of histone deacetylase. The prodrugs of the present invention have good aqueous solubility and good aqueous stability. The prodrugs of the invention advantageously are metabolized to the active i

Prodrugs of Compounds that Enhance Antifungal Activity and Compositions of Said Prodrugs

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Paragraph 0357; 0358; 0374, (2015/07/27)

The invention relates to prodrugs for use in the inhibition of histone deacetylase. The prodrugs of the present invention have good aqueous solubility and good aqueous stability. The prodrugs of the invention advantageously are metabolized to the active i

Direct C-H alkylation of naphthoquinones with amino acids through a revisited Kochi-Anderson radical decarboxylation: Trends in reactivity and applications

Naturale, Guillaume,Lamblin, Marc,Commandeur, Claude,Dessolin, Jean,Felpin, Francois-Xavier

supporting information, p. 5774 - 5788,15 (2020/09/15)

In our ongoing research program into the discovery of new anticancer drugs, we were interested in the preparation of naphthoquinone scaffolds bearing aminoalkyl side-chains. Following this aim, we revisited the Kochi-Anderson radical decarboxylation of amino acids in order to set up a versatile route to the direct functionalization of naphthoquinones. The best reaction conditions were applied to a selected series of compounds in a systematic methodological study which allowed us to establish important trends in reactivity. We found that α-substituted β-amino acids were the most suitable substrates for the radical addition. In contrast, α-amino acids gave modest results. The influence of the amine protecting groups on the reaction outcome has also been studied. This practical procedure allows the introduction of various unsymmetrical moieties, including orthogonally protected linear aminoalkyl chains or chiral dipeptidic chains, and opens the door to a wide scope of easily accessible chemical diversity.

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