324752-72-9

Basic information

• Product Name: Carbamic acid, [(1R,2S)-2-hydroxy-1-methyl-4-pentenyl]-, 1,1-dimethylethyl
• Synonyms: Carbamic acid, [(1R,2S)-2-hydroxy-1-methyl-4-pentenyl]-, 1,1-dimethylethyl
• CAS NO: 324752-72-9
• Molecular Formula: C11H21NO3
• Molecular Weight: 215.28934
• Product Categories: N-BOC
• Mol File: 324752-72-9.mol
• Article Data: 12

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Carbamic acid, [(1R,2S)-2-hydroxy-1-methyl-4-pentenyl]-, 1,1-dimethylethyl(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, [(1R,2S)-2-hydroxy-1-methyl-4-pentenyl]-, 1,1-dimethylethyl(324752-72-9)
• EPA Substance Registry System: Carbamic acid, [(1R,2S)-2-hydroxy-1-methyl-4-pentenyl]-, 1,1-dimethylethyl(324752-72-9)

Safety Data

• Hazardous Substances Data: 324752-72-9(Hazardous Substances Data)

Upstream product

• 1294446-91-5 (S)-tert-butyl-N-(3-oxohex-5-en-2-yl)carbamate 
• 15761-38-3 L-N-Boc-Ala 
• 24424-99-5 di-tert-butyl dicarbonate 
• 82353-56-8 (2R)-2-N-t-butoxycarbonyl-aminopropanal 
• 762-72-1 allyl-trimethyl-silane 
• 174787-76-9 (4R,5R)-5-allyl-3-tert-butoxycarbonyl-4-methyl-2-oxazolidinone 
• 7393-43-3 tetraallyl tin 
• 146553-06-2 tert-butyl {(S)-1-[methoxy(methyl)amino]-1-oxopropan-2-yl}carbamate 
• 79069-50-4 Boc-Ala-H 
• 85116-38-7 (-)-B-allyldiisopinocampheylborane 
• 1730-25-2 allylmagnesium bromide 
• 107-37-9 allyltrichlorosilane 
• 106-95-6 allyl bromide 
• 174851-37-7 (4R,5R)-5-allyl-4-methyl-2-oxazolidinone 

Relevant articles and documents

A simple one pot procedure for the generation of homoallylic alcohols from acetals and amino acids

Treatment of acetals (1 and 2) and amino acetals (3-5) with either trifluoroacetic acid (TFA) or silica gel followed by tetraallyltin gave excellent yields of the corresponding homoallylic alcohols (68 - 100%).

PYRIMIDINE CARBOXAMIDES AS GSK-3 INHIBITORS

The disclosure generally relates to compounds of formula I, including their salts, as well as compositions and methods of using the compounds to treat disorders associated with GSK-3.

A facile approach to trans-4,5-pyrrolidine lactam and application in the synthesis of nemonapride and streptopyrrolidine

An efficient approach to trans-4-hydroxylpyrrolidine lactams 1 starting from amino acid is described. The utility of this method has been demonstrated in the synthesis of antipsychotic nemonapride 3 and antiangiogenic streptopyrrolidine 4. Compared four s