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1-Azabicyclo[2.2.2]octane-2-methanamine,5-ethynyl-,(1S,2S,4S,5S)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

475160-60-2

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475160-60-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 475160-60-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,5,1,6 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 475160-60:
(8*4)+(7*7)+(6*5)+(5*1)+(4*6)+(3*0)+(2*6)+(1*0)=152
152 % 10 = 2
So 475160-60-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H16N2/c1-2-8-7-12-4-3-9(8)5-10(12)6-11/h1,8-10H,3-7,11H2/t8-,9-,10-/m0/s1

475160-60-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (1S,2S,4S,5R)-2-(aminoethyl)-5-ethynyl-1-azabicyclo[2.2.2]octane

1.2 Other means of identification

Product number -
Other names C-((1S,2S,4S,5S)-5-Ethynyl-1-aza-bicyclo[2.2.2]oct-2-yl)-methylamine

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:475160-60-2 SDS

475160-60-2Upstream product

475160-60-2Downstream Products

475160-60-2Relevant academic research and scientific papers

New hydrogenated and didehydrogenated 1,2-diamines of quincorine and quincoridine

Neda, Ion,Kaukorat, Thomas,Hrib, Christian

, p. 1327 - 1330 (2002)

Four new members of the family of 1,2-diamines of quincorine and quincoridine have been synthesized, being hydrogenated and didehydrogenated at the C10-C11 fragment. The alkynes, containing an additional amino group at C9, are potentially useful building blocks for cross-coupling reactions. Additional investigations concerning the chemical properties of the molecules point to a significant impact of the remote C5 substituent on the basicity of the bridgehead nitrogen.

Unusual stabilization of 1,2-diamino derivatives of quincorine and quincoridine by carbon dioxide: Persistent crystalline prim-ammonium-carbamate salts and their reactivity towards isatoic acid anhydride

Neda, Ion,Kaukorat, Thomas,Fischer, Axel K.

, p. 3784 - 3790 (2007/10/03)

The reaction of N-methylisatoic anhydride 1 with a series of quincorine (QCI) and quincoridine (QCD) derivatives furnished the corresponding QCI- and QCD-substituted anthranilic acid amides 4-9. In the synthesis of 4-9, we investigated the influence of th

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