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1H-Azepine,hexahydro-2-(2-pyridinyl)-
Cas No: 383128-97-0
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1 Gram
1 Metric Ton/Day
Shandong Mopai Biotechnology Co., LTD
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1H-Azepine,hexahydro-2-(2-pyridinyl)-
Cas No: 383128-97-0
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Antimex Chemical Limied
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2-PYRIDIN-2-YL-AZEPANE
Cas No: 383128-97-0
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ZHEJIANG JIUZHOU CHEM CO.,LTD
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1H-Azepine,hexahydro-2-(2-pyridinyl)-
Cas No: 383128-97-0
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InFarmatik Bt.
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383128-97-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 383128-97-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,3,1,2 and 8 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 383128-97:
(8*3)+(7*8)+(6*3)+(5*1)+(4*2)+(3*8)+(2*9)+(1*7)=160
160 % 10 = 0
So 383128-97-0 is a valid CAS Registry Number.

InChI:InChI=1/C11H16N2/c1-2-6-10(12-8-4-1)11-7-3-5-9-13-11/h3,5,7,9-10,12H,1-2,4,6,8H2/p+1/t10-/m1/s1

383128-97-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name	2-pyridin-2-ylazepane

1.2 Other means of identification

Product number	-
Other names	-

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:383128-97-0 SDS

383128-97-0Upstream product

383128-97-0Downstream Products

383128-97-0Relevant articles and documents

Chemoenzymatic Synthesis of Substituted Azepanes by Sequential Biocatalytic Reduction and Organolithium-Mediated Rearrangement

Zawodny, Wojciech,Montgomery, Sarah L.,Marshall, James R.,Finnigan, James D.,Turner, Nicholas J.,Clayden, Jonathan

supporting information, p. 17872 - 17877 (2019/01/04)

Enantioenriched 2-aryl azepanes and 2-arylbenzazepines were generated biocatalytically by asymmetric reductive amination using imine reductases or by deracemization using monoamine oxidases. The amines were converted to the corresponding N′-aryl ureas, which rearranged on treatment with base with stereospecific transfer of the aryl substituent to the 2-position of the heterocycle via a configurationally stable benzyllithium intermediate. The products are previously inaccessible enantioenriched 2,2-disubstituted azepanes and benzazepines.

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CAS

383128-97-0