(R)-2-Pyrrolidineboronicacidpinanediolesterhydrochloride
(R)-BoroPro-(+)-Pinanediol-HCl
CAS: 147208-69-3
Molecular Formula: C14H24BNO2.ClH
(R)-2-Pyrrolidineboronicacidpinanediolesterhydrochloride - Names and Identifiers
| Name | (R)-BoroPro-(+)-Pinanediol-HCl |
| Synonyms | (R)-BoroPro-(+)-Pinediol-HCl (R)-BoroPro-(+)-Pinanediol-HCl (R)-BoroPro-(+)-Pinanediol-hydrochloride (r)-2-pyrrolidineboronic acid pinanediol ester (R)-2-Pyrrolidineboronicacidpinanediolesterhydrochloride (R)-1H-Pyrrolidine-2-boronic acid, pinanediol ester, HCl (R)-2-Pyrrolidineboronic acid pinanediol ester hydrochloride (R)-2-((3aS,4S,6S,7aR)-3a,5,5-TriMethylhexahydro-4,6-Methanobenzo[d][1,3,2]dioxaborol-2-yl)pyrrolidine hydrochloride |
| CAS | 147208-69-3 |
| InChI | InChI=1/C14H24BNO2.ClH/c1-13(2)9-7-10(13)14(3)11(8-9)17-15(18-14)12-5-4-6-16-12;/h9-12,16H,4-8H2,1-3H3;1H/t9-,10-,11+,12-,14-;/m0./s1 |
(R)-2-Pyrrolidineboronicacidpinanediolesterhydrochloride - Physico-chemical Properties
| Molecular Formula | C14H24BNO2.ClH |
| Molar Mass | 285.621 |
| Storage Condition | Sealed in dry,Room Temperature |
(R)-2-Pyrrolidineboronicacidpinanediolesterhydrochloride - Introduction
(R)-BoroPro-( )-Pinanediol-HCl, also known as (R)-PipBPin · HCl, is a compound with the following properties:
1. Appearance: white solid.
2. Melting Point: about 125-127 ° C.
3. Solubility: soluble in some organic solvents, such as dimethyl sulfoxide and dimethylformamide.
4. Structure: The compound has Topological chirality and can be used as a catalyst for cysteine residue pseudoenzyme (Sa-FadD32S).
The compound has a wide range of applications in chemical research, mainly including the following aspects:
1. Catalyst: It can be used as a catalyst for cysteine residue pseudo-enzyme (Sa-FadD32S) to catalyze chiral esterification and amino acid esterification.
2. Fine chemicals synthesis: for the synthesis of drugs and organic compounds with chiral environment.
3. Drug research: as a drug synthesis intermediate, used in the synthesis of chiral drugs.
The method of preparing (R)-PipBPin · HCl usually involves the following steps:
1. Synthesis of (R)-2-pyrrolidine boronic acid pinanediol ester: Obtain by reacting (R)-2-pyrrolidine with dimethyl borate.
2. Preparation of Hydrochloride: (R)-2-pyrrolidine boronic acid pinanediol Ester is reacted with hydrochloric acid to generate (R)-PipBPin · HCl.
Regarding safety information, due to the application of (R)-PipBPin · HCl in chemical laboratories, appropriate safety measures need to be taken:
1. Avoid inhalation: it should be operated in a well-ventilated place to avoid inhalation of dust or steam.
2. Avoid contact with skin and eyes: Wear appropriate personal protective equipment, such as gloves and goggles, when using the compound.
3. Storage: The compound should be stored in a sealed container, avoiding contact with air and moisture.
1. Appearance: white solid.
2. Melting Point: about 125-127 ° C.
3. Solubility: soluble in some organic solvents, such as dimethyl sulfoxide and dimethylformamide.
4. Structure: The compound has Topological chirality and can be used as a catalyst for cysteine residue pseudoenzyme (Sa-FadD32S).
The compound has a wide range of applications in chemical research, mainly including the following aspects:
1. Catalyst: It can be used as a catalyst for cysteine residue pseudo-enzyme (Sa-FadD32S) to catalyze chiral esterification and amino acid esterification.
2. Fine chemicals synthesis: for the synthesis of drugs and organic compounds with chiral environment.
3. Drug research: as a drug synthesis intermediate, used in the synthesis of chiral drugs.
The method of preparing (R)-PipBPin · HCl usually involves the following steps:
1. Synthesis of (R)-2-pyrrolidine boronic acid pinanediol ester: Obtain by reacting (R)-2-pyrrolidine with dimethyl borate.
2. Preparation of Hydrochloride: (R)-2-pyrrolidine boronic acid pinanediol Ester is reacted with hydrochloric acid to generate (R)-PipBPin · HCl.
Regarding safety information, due to the application of (R)-PipBPin · HCl in chemical laboratories, appropriate safety measures need to be taken:
1. Avoid inhalation: it should be operated in a well-ventilated place to avoid inhalation of dust or steam.
2. Avoid contact with skin and eyes: Wear appropriate personal protective equipment, such as gloves and goggles, when using the compound.
3. Storage: The compound should be stored in a sealed container, avoiding contact with air and moisture.
Last Update：2024-04-09 21:04:16
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