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131667-57-7

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131667-57-7 Usage

General Description

N-Boc-3,4-dihydro-2H-pyridine is a chemical compound with the molecular formula C13H19NO2. It is also known as tert-butyl 3,4-dihydro-2H-pyridine-1-carboxylate. N-Boc-3,4-dihydro-2H-pyridine is commonly used as an intermediate in organic synthesis and pharmaceutical research. It serves as a key building block in the production of various pharmaceuticals and agrochemicals. N-Boc-3,4-dihydro-2H-pyridine is a white or off-white solid that is soluble in organic solvents such as dichloromethane and ethyl acetate. It is important to handle this compound with caution and use proper safety measures, as it may pose health hazards if not handled properly.

Check Digit Verification of cas no

The CAS Registry Mumber 131667-57-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,6,6 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 131667-57:
(8*1)+(7*3)+(6*1)+(5*6)+(4*6)+(3*7)+(2*5)+(1*7)=127
127 % 10 = 7
So 131667-57-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H17NO2/c1-10(2,3)13-9(12)11-7-5-4-6-8-11/h5,7H,4,6,8H2,1-3H3

131667-57-7 Well-known Company Product Price

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  • Aldrich

  • (715239)  N-Boc-3,4-dihydro-2H-pyridine  97%

  • 131667-57-7

  • 715239-1G

  • 704.34CNY

  • Detail
  • Aldrich

  • (715239)  N-Boc-3,4-dihydro-2H-pyridine  97%

  • 131667-57-7

  • 715239-1G

  • 704.34CNY

  • Detail
  • Aldrich

  • (715239)  N-Boc-3,4-dihydro-2H-pyridine  97%

  • 131667-57-7

  • 715239-1G

  • 704.34CNY

  • Detail
  • Aldrich

  • (715239)  N-Boc-3,4-dihydro-2H-pyridine  97%

  • 131667-57-7

  • 715239-1G

  • 704.34CNY

  • Detail

131667-57-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 3,4-dihydro-2H-pyridine-1-carboxylate

1.2 Other means of identification

Product number -
Other names 1-N-Boc-3,4-dihydro-2H-pyridine

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:131667-57-7 SDS

131667-57-7Downstream Products

131667-57-7Relevant articles and documents

A facile synthesis of cyclic enecarbamates using Dess-Martin periodinane

Yu, Chengzhi,Hu, Longqin

, p. 5167 - 5170 (2001)

A simple and efficient synthesis of cyclic enecarbamates from ω-hydroxycarbamates via tandem oxidative cyclization-dehydration was achieved in 84% to quantitative yield using Dess-Martin periodinane in methylene chloride.

Backbone-Modified C2-Symmetrical Chiral Bisphosphine TMS-QuinoxP*: Asymmetric Borylation of Racemic Allyl Electrophiles

Imamoto, Tsuneo,Ito, Hajime,Iwamoto, Hiroaki,Ozawa, Yu,Takenouchi, Yuta

supporting information, p. 6413 - 6422 (2021/05/31)

A new C2-symmetrical P-chirogenic bisphosphine ligand with silyl substituents on the ligand backbone, (R,R)-5,8-TMS-QuinoxP*, has been developed. This ligand showed higher reactivity and enantioselectivity for the direct enantioconvergent borylation of cy

Merging Halogen-Atom Transfer (XAT) and Cobalt Catalysis to Override E2-Selectivity in the Elimination of Alkyl Halides: A Mild Route towardcontra-Thermodynamic Olefins

Zhao, Huaibo,McMillan, Alastair J.,Constantin, Timothée,Mykura, Rory C.,Juliá, Fabio,Leonori, Daniele

supporting information, p. 14806 - 14813 (2021/09/18)

We report here a mechanistically distinct tactic to carry E2-type eliminations on alkyl halides. This strategy exploits the interplay of α-aminoalkyl radical-mediated halogen-atom transfer (XAT) with desaturative cobalt catalysis. The methodology is high-yielding, tolerates many functionalities, and was used to access industrially relevant materials. In contrast to thermal E2 eliminations where unsymmetrical substrates give regioisomeric mixtures, this approach enables, by fine-tuning of the electronic and steric properties of the cobalt catalyst, to obtain high olefin positional selectivity. This unprecedented mechanistic feature has allowed access tocontra-thermodynamic olefins, elusive by E2 eliminations.

?-C(sp2)-H alkylation of enamides using xanthate chemistry

Bertho, Sylvain,Dondasse, Isma?l,Retailleau, Pascal,Nicolas, Cyril,Gillaizeau, Isabelle

supporting information, p. 7129 - 7141 (2020/05/16)

Access to the ?-amino-?,?-unsaturated acyl scaffold was established by applying xanthate chemistry to enamides. This original ?-C(sp2)-H alkylation is regioselective and exhibits broad substrate scope and good functional group tolerance. The la

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