13734-32-2Relevant articles and documents
Improved synthesis of etert-butyloxycarbonyl-amino acids through pH stable reactions
Schnabel
, p. 188 - 196 (1967)
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13734-32-2
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Basic information
- Product Name: 2-(tert-butoxycarbonyl-methyl-amino)-4-methyl-pentanoic acid
- Synonyms: 2-(tert-butoxycarbonyl-methyl-amino)-4-methyl-pentanoic acid
- CAS NO:13734-32-2
- Molecular Formula:
- Molecular Weight: 245.319
- EINECS: N/A
- Product Categories: N/A
- Mol File: 13734-32-2.mol
- Article Data: 1
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Chemical Properties
- Melting Point: N/A
- Boiling Point: N/A
- Flash Point: N/A
- Appearance: N/A
- Density: N/A
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: 2-(tert-butoxycarbonyl-methyl-amino)-4-methyl-pentanoic acid(CAS DataBase Reference)
- NIST Chemistry Reference: 2-(tert-butoxycarbonyl-methyl-amino)-4-methyl-pentanoic acid(13734-32-2)
- EPA Substance Registry System: 2-(tert-butoxycarbonyl-methyl-amino)-4-methyl-pentanoic acid(13734-32-2)
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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: 13734-32-2(Hazardous Substances Data)
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13734-32-2 Usage
Molecular structure
2-(tert-butoxycarbonyl-methyl-amino)-4-methyl-pentanoic acid has a complex molecular structure, which includes a pentanoic acid backbone with a methyl-amino group and a tert-butoxycarbonyl (Boc) protecting group attached to the amino group.Derivative of valine
This compound is a derivative of the amino acid valine, which means it is structurally related to valine but has been modified to include additional functional groups.Use in organic synthesis
2-(tert-butoxycarbonyl-methyl-amino)-4-methyl-pentanoic acid is commonly used as a building block in the preparation of peptides and other bioactive molecules, making it a valuable compound in the field of organic synthesis.Stability
The compound is known for its stability, which is important for its use in synthetic processes, as it helps prevent unwanted side reactions and degradation.Protection of amine group
The presence of the Boc protecting group in the compound helps protect the amine group from unwanted reactions during synthetic processes, ensuring that the desired product is obtained with minimal impurities and side products.Selective deprotection
The Boc group in 2-(tert-butoxycarbonyl-methyl-amino)-4-methyl-pentanoic acid allows for selective deprotection, meaning that the protecting group can be removed under specific conditions without affecting other functional groups in the molecule. This enables further modification and customization of the compound for specific research or industrial applications.Check Digit Verification of cas no
The CAS Registry Mumber 13734-32-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,7,3 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.Calculate Digit Verification of CAS Registry Number 13734-32:
(7*1)+(6*3)+(5*7)+(4*3)+(3*4)+(2*3)+(1*2)=92
92 % 10 = 2
So 13734-32-2 is a valid CAS Registry Number.
13734-32-2Upstream product
13734-32-2Downstream Products
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2-(tert-butoxycarbonyl-methyl-amino)-4-methyl-pentanoic acid
