logo
Home  > Chemistry  > Organic Building Blocks  > Aliphatic Chain Hydrocarbons  > (3-Chloro-propyl)-methyl-carbamic acid tert-butyl ester

AA14189

114326-14-6 | (3-Chloro-propyl)-methyl-carbamic acid tert-butyl ester

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $70.00 $49.00 -   +
250mg 95% in stock $95.00 $66.00 -   +
1g 95% in stock $174.00 $122.00 -   +
5g 95% in stock $611.00 $428.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AA14189
Chemical Name: (3-Chloro-propyl)-methyl-carbamic acid tert-butyl ester
CAS Number: 114326-14-6
Molecular Formula: C9H18ClNO2
Molecular Weight: 207.69772
MDL Number: MFCD09031544
SMILES: ClCCCN(C(=O)OC(C)(C)C)C

 

Computed Properties
Complexity: 166  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 13  
Hydrogen Bond Acceptor Count: 2  
Rotatable Bond Count: 5  
XLogP3: 2.1  

 

 

Upstream Synthesis Route
  • The tert-Butyl (3-chloropropyl)(methyl)carbamate is a versatile compound commonly used in chemical synthesis as a key building block for the preparation of various agrochemicals, pharmaceuticals, and specialty chemicals. Its unique structure and reactivity allow for efficient and selective derivatization, making it a valuable reagent in organic synthesis.When used in chemical reactions, tert-Butyl (3-chloropropyl)(methyl)carbamate acts as a source of both the 3-chloropropyl and methyl functional groups, enabling the introduction of these specific moieties into target molecules with precision. This controlled functionalization is crucial in the development of new compounds with desired properties and activities.In addition to its role as a synthetic intermediate, tert-Butyl (3-chloropropyl)(methyl)carbamate can also serve as a protecting group for amines in complex multi-step syntheses. By temporarily masking the amino functionality, this compound helps to prevent unwanted side reactions and ensures the desired regioselectivity and stereochemistry in the final product.Overall, the application of tert-Butyl (3-chloropropyl)(methyl)carbamate in chemical synthesis demonstrates its importance as a versatile building block and protective group, enabling the efficient and strategic design of novel compounds with diverse applications.
FEATURED PRODUCTS