131971-63-6

Basic information

• Product Name: Carbamic acid, (1-methoxy-2-methylpropyl)-, 1,1-dimethylethyl ester (9CI)
• Synonyms: Carbamic acid, (1-methoxy-2-methylpropyl)-, 1,1-dimethylethyl ester (9CI)
• CAS NO: 131971-63-6
• Molecular Formula: C₁₀H₂₁NO₃
• Molecular Weight: 203.27864
• Product Categories: N-BOC
• Mol File: 131971-63-6.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Carbamic acid, (1-methoxy-2-methylpropyl)-, 1,1-dimethylethyl ester (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, (1-methoxy-2-methylpropyl)-, 1,1-dimethylethyl ester (9CI)(131971-63-6)
• EPA Substance Registry System: Carbamic acid, (1-methoxy-2-methylpropyl)-, 1,1-dimethylethyl ester (9CI)(131971-63-6)

Safety Data

• Hazardous Substances Data: 131971-63-6(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 317359-30-1 tert-butyl 2-methylpropylidenecarbamate 
• 13734-41-3 t-Boc-L-valine 
• 91230-06-7 3--2-methylprop-1-ene 
• 13734-41-3 N-Boc-(S/R)-valine 

Relevant articles and documents

Catalyst-free Mannich-type reaction of 1-(N-acylamino)alkyltriphenylphosphonium salts with silyl enolates

A catalyst-free reaction of 1-(N-acylamino)alkyltriphenylphosphonium tetrafluoroborates with silyl enolates was developed to prepare β-amino carbonyl compounds. The reported method is a useful approach for the preparation of N-protected β-amino esters as

1-(N -acylamino)alkyl sulfones from N -acyl-α-amino acids or N -alkylamides

A variety of N-(1-methoxyalkyl)amides or carbamates react readily with sodium aryl sulfinates in the presence of triphenylphosphonium tetrafluoroborate or bromide in CHCl3 under mild conditions to give 1-(N-acylamino)alkyl sulfones in good yiel

Activation of hemiaminal ethers by chiral broensted acids for facile access to enantioselective two-carbon homologation using eneearbamates

-