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Tert-butyl 4-hydroxy-4-vinylpiperidine-1-carboxylate is a chemical compound with the molecular formula C13H23NO3. It is a derivative of piperidine, a heterocyclic amine, and contains both a tert-butyl group and a vinyl group. This versatile and valuable compound is widely used in the field of organic chemistry.
Used in Organic Synthesis:
Tert-butyl 4-hydroxy-4-vinylpiperidine-1-carboxylate is used as a reactant in organic synthesis for its ability to undergo various reactions to produce different compounds. Its presence of both a tert-butyl group and a vinyl group allows for a range of synthetic applications.
Used in Peptide Synthesis:
In the field of peptide synthesis, tert-butyl 4-hydroxy-4-vinylpiperidine-1-carboxylate is used as a protective group for the amine group of an amino acid. This function is crucial to prevent undesired reactions during peptide bond formation, ensuring the successful synthesis of the desired peptide sequence.

371975-46-1

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371975-46-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 371975-46-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,1,9,7 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 371975-46:
(8*3)+(7*7)+(6*1)+(5*9)+(4*7)+(3*5)+(2*4)+(1*6)=181
181 % 10 = 1
So 371975-46-1 is a valid CAS Registry Number.

371975-46-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-ethenyl-4-hydroxypiperidine-1-carboxylic acid 1,1-dimethylethyl ester

1.2 Other means of identification

Product number -
Other names tert-butyl 4-hydroxy-4-vinylpiperidine-1-carboxylate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:371975-46-1 SDS

371975-46-1Downstream Products

371975-46-1Relevant articles and documents

Catalytic Radical-Polar Crossover Reactions of Allylic Alcohols

Touney, Eric E.,Foy, Nicholas J.,Pronin, Sergey V.

supporting information, p. 16982 - 16987 (2018/12/14)

Radical-polar crossover hydrofunctionalizations of tertiary allylic alcohols are described. Depending on the structure of the catalyst, corresponding epoxides or semipinacol rearrangement products are selectively obtained in good yields. Experimental evidence points to the participation of alkylcobalt complexes as electrophilic intermediates.

N-LINKED LACTAM M1 RECEPTOR POSITIVE ALLOSTERIC MODULATORS

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Page/Page column 57, (2012/12/13)

The present invention is directed to N-linked lactam compounds of general formula (I) which are M1 receptor positive allosteric modulators and that are useful in the treatment of diseases in which the M1 receptor is involved, such as Alzheimer's disease, schizophrenia, pain or sleep disorders. The invention is also directed to pharmaceutical compositions comprising the compounds, and to the use of the compounds and compositions in the treatment of diseases mediated by the M1 receptor.

PYRAZOLO PYRIMIDINE DERIVATIVES

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Paragraph 0332-0333, (2013/03/26)

The present invention relates to pyrazolo pyrimidine derivatives, to methods of preparing these, to combinations and pharmaceutical composition comprising these, and to their use in the treatment of diseases and disorders which may for example involve autoimmune diseases, angiogenesis, pain, and/or inflammatory diseases.

Synthesis of carbo- and heterocyclic aldehydes bearing an adjacent donor group - Ozonolysis versus OsO4/KIO4-oxidation

Mihovilovic, Marko D.,Spina, Markus,Mueller, Bernhard,Stanetty, Peter

, p. 899 - 909 (2007/10/03)

The synthesis of carbo- and heterocyclic aldehydes bearing an ipso-methoxy group is investigated. The synthetic sequence is based on an initial Grignard addition of an olefin to a cyclic ketone followed by methylation of the resulting tertiary alcohol. The terminal olefin serves as precursor for the aldehyde functionality. Oxidation by ozonolysis turned out to depend significantly on the distance of the donor methoxy group. The observed side reactions could be circumvented by applying a one-pot OsO4 mediated diol formation followed by Malaprade oxidation using KIO4. A series of carbo- and heterocyclic precursors were successfully converted to the title products. Springer-Verlag 2004.

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