2-(tert-butoxycarbonylaMino)-4,4-diMethylpentanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.
507264-54-2
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Basic information
- Product Name: 2-(tert-butoxycarbonylaMino)-4,4-diMethylpentanoic acid
- Synonyms: 2-(tert-butoxycarbonylaMino)-4,4-diMethylpentanoic acid;Boc-b-tert-butyl-DL-alanine;N-BOC-3-T-BUTYL-DL-ALANINE
- CAS NO:507264-54-2
- Molecular Formula: C12H23NO4
- Molecular Weight: 245.31532
- EINECS: N/A
- Product Categories: N/A
- Mol File: 507264-54-2.mol
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Chemical Properties
- Melting Point: N/A
- Boiling Point: 364.4±25.0 °C(Predicted)
- Flash Point: N/A
- Appearance: /
- Density: 1.048±0.06 g/cm3(Predicted)
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- PKA: 4.03±0.23(Predicted)
- CAS DataBase Reference: 2-(tert-butoxycarbonylaMino)-4,4-diMethylpentanoic acid(CAS DataBase Reference)
- NIST Chemistry Reference: 2-(tert-butoxycarbonylaMino)-4,4-diMethylpentanoic acid(507264-54-2)
- EPA Substance Registry System: 2-(tert-butoxycarbonylaMino)-4,4-diMethylpentanoic acid(507264-54-2)
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Safety Data
- Hazard Codes: N/A
- Statements: N/A
- Safety Statements: N/A
- WGK Germany:
- RTECS:
- HazardClass: N/A
- PackingGroup: N/A
- Hazardous Substances Data: 507264-54-2(Hazardous Substances Data)
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507264-54-2 Usage
Molecular structure
The compound has a valine derivative structure with a tert-butoxycarbonyl (Boc) protecting group attached to the amino group and a branched, 4,4-dimethylpentanoic acid moiety.Functional groups
The compound contains an amino group, a tert-butoxycarbonyl (Boc) group, and a carboxylic acid group.Protecting group
The Boc group attached to the amino group serves as a protecting group, allowing for selective manipulation of the amino group during chemical reactions.Steric hindrance
The 4,4-dimethylpentanoic acid moiety provides steric hindrance, which can be useful for controlling the selectivity of chemical reactions.Chemical properties
The compound has unique chemical properties due to the presence of the Boc protecting group and the branched, 4,4-dimethylpentanoic acid moiety.Synthesis
The compound is commonly used as a building block in organic synthesis and medicinal chemistry for the synthesis of complex organic molecules and pharmaceutical compounds.Check Digit Verification of cas no
The CAS Registry Mumber 507264-54-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,7,2,6 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.Calculate Digit Verification of CAS Registry Number 507264-54:
(8*5)+(7*0)+(6*7)+(5*2)+(4*6)+(3*4)+(2*5)+(1*4)=142
142 % 10 = 2
So 507264-54-2 is a valid CAS Registry Number.
InChI:InChI=1S/C12H23NO4/c1-11(2,3)7-8(9(14)15)13-10(16)17-12(4,5)6/h8H,7H2,1-6H3,(H,13,16)(H,14,15)
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2-(tert-butoxycarbonylaMino)-4,4-diMethylpentanoic acid
