Learn More
Description
- 1-chloro-3-iodopropane undergoes asymmetric α-alkylation with n-sulfinyl imidates to yield 2-substituted n-tert-butanesulfinyl-5-chloropentanimidates. electroreduction of 1-chloro-3-iodopropane at glassy carbon electrode in dimethylformamide containing tetra-n-butylammonium perchlorate has been investigated by cyclic voltammetry. it also participates in conjugate addition of alkyl iodides to α,α-unsaturated nitriles in water.1-chloro-3-iodopropane has been used in the synthesis of:
- N-[4-[5-(2,4-diamino-6-oxo-1,6-dihydropyrimidin-5-yl)-2-(2,2,2-trifluoroacetyl)pentyl]benzoyl]-L-glutamic acid, an inhibitor of glycinamide ribonucleotide transformylase (gar tfase) and aminoimidazole carboxamide ribonucleotide transformylase (aicar tfase)
- Interesting αproton spongeα type molecule quino[7,8-h]quinoline
Specifications
Specifications
| CAS | 871-91-0 |
| Molecular Formula | C8H14O |
| Linear Formula | C8H14O |
| MDL Number | MFCD01632137 |
| Quantity | 100 g |
| Molecular Weight (g/mol) | 126.2 |
By clicking Submit, you acknowledge that you may be contacted by Fisher Scientific in regards to the feedback you have provided in this form. We will not share your information for any other purposes. All contact information provided shall also be maintained in accordance with our Privacy Policy.