167479-01-8
167479-01-8
Chemical Structure
tert-Butyl 3-iodopropylcarbamate
- CAS No.: 167479-01-8
- Formula:C8H16INO2
- Molecular Weight:285.12
IUPAC Name: tert-butyl (3-iodopropyl)carbamate
InChIKey: ORVXNBKOWDNMGB-UHFFFAOYSA-N
SMILES: O=C(NCCCI)OC(C)(C)C
Biological Activity: tert-Butyl 3-iodopropylcarbamate is a compound with a t-butyl and a terminal iodine. The iodine (I) is a very good leaving group for nucleophilic substitution reactions. The Boc group can be deprotected under mild acidic conditions to form the free amine.
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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tert-Butyl 3-iodopropylcarbamate | tert-Butyl 3-iodopropylcarbamate is a compound with a t-butyl and a terminal iodine. The iodine (I) is a very good leaving group for nucleophilic substitution reactions. The Boc group can be deprotected under mild acidic conditions to form the free amine. | |||||||||||||||||||||
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Boc-β-Ala-ol | 99.76% | Boc-β-Ala-ol (3-(Boc-amino)-1-propanol) is an alanine derivative with a Boc protecting group at the N-terminus, which can be used to synthesize bioactive peptide mimics, such as Nα-Benzoyl-α-azaornithine phenyl ester, which has trypsin inhibitory activity. | ||||||||||||||||||||
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tert-Butyl (3-aminopropyl)carbamate | 99.82% | tert-Butyl (3-aminopropyl)carbamate is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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3-(Boc-amino)propyl bromide | 99.95% | 3-(Boc-amino) propyl bromide is an alkylating reagent used for the N-alkylation of benzopyranotriazolopyrimidine-based MDM2-p53 protein-protein inhibitor 4 to prepare Compound 13. | ||||||||||||||||||||
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tert-Butyl (3-aminopropyl)carbamate hydrochloride | tert-Butyl (3-aminopropyl)carbamate hydrochloride is a PROTAC linker that can be used in the synthesis of PROTACs. | |||||||||||||||||||||
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tert-Butyl (2-iodoethyl)carbamate | 99.89% | tert-Butyl (2-iodoethyl)carbamate is a PROTAC linker that can be used in the synthesis of PROTACs. | ||||||||||||||||||||
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tert-Butyl (3-chloropropyl)carbamate | 99.49% | tert-Butyl (3-chloropropyl)carbamate is a compound with a t-butyl and a terminal choloride. The cholorine (Cl) is a good leaving group for nucleophilic substitution reactions. The Boc group can be deprotected under mild acidic conditions to form the free amine. | ||||||||||||||||||||
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tert-Butyl (4-iodobutyl)carbamate | tert-Butyl (4-iodobutyl)carbamate is a four carbon linker containing a Boc-protected amino group and an iodine group. The Boc group can be deprotected under mild acidic conditions to form the free amine. Iodine (I) is a very good leaving group for nucleophilic substitution reactions. | |||||||||||||||||||||
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tert-Butyl (5-iodopentyl)carbamate | tert-Butyl (5-iodopentyl)carbamate is a PROTAC linker that can be used in the synthesis of PROTACs. | |||||||||||||||||||||
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tert-Butyl (6-iodohexyl)carbamate | tert-Butyl (6-iodohexyl)carbamate is a six carbon linker containing an iodine group and a t-butyl ester. The iodine (I) acts as a good leaving group for nucleophilic substitution reactions. The t-butyl ester groups can be deprotected under acidic conditions. | |||||||||||||||||||||
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tert-Butyl (2-(2-iodoethoxy)ethyl)carbamate | ≥97.0% | tert-Butyl (2-(2-iodoethoxy)ethyl)carbamate is a PROTAC linker that can be used in the synthesis of PROTACs. | ||||||||||||||||||||
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