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18595-55-6

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18595-55-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18595-55-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,5,9 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 18595-55:
(7*1)+(6*8)+(5*5)+(4*9)+(3*5)+(2*5)+(1*5)=146
146 % 10 = 6
So 18595-55-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H15NO3/c1-14(2,3)18-13(16)17-11-8-4-6-10-7-5-9-15-12(10)11/h4-9H,1-3H3

18595-55-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl quinolin-8-yl carbonate

1.2 Other means of identification

Product number -
Other names O-tert-butoxycarbonyl-8-hydroxyquinoline

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:18595-55-6 SDS

18595-55-6Relevant articles and documents

Site-selective C-H borylation of quinolines at the C8 position catalyzed by a silica-supported phosphane-iridium system

Konishi, Shota,Kawamorita, Soichiro,Iwai, Tomohiro,Steel, Patrick G.,Marder, Todd B.,Sawamura, Masaya

supporting information, p. 434 - 438 (2014/02/14)

Site-selective C-H borylation of quinoline derivatives at the C8 position has been achieved by using a heterogeneous Ir catalyst system based on a silica-supported cage-type monophosphane ligand SMAP. The efficient synthesis of a corticotropin-releasing f

Di-tert-butyl dicarbonate and 4-(dimethylamino)pyridine revisited. Their reactions with amines and alcohols

Basel, Yochai,Hassner, Alfred

, p. 6368 - 6380 (2007/10/03)

The reaction of BOC2O in the presence and absence of DMAP was examined with some amines, alcohols, diols, amino alcohols, and aminothiols. Often, unusual products were observed depending on the ratio of reagents, reaction time, polarity of solvent, pK(a) of alcohols, or type of amine (primary or secondary). In reactions of aliphatic alcohols with BOC2O/DMAP, we isolated for the first time carbonic-carbonic anhydride intermediates; this helps explain the formation of symmetrical carbonates in addition to the O-BOC products. In the case of secondary amines, we succeeded to isolate unstable carbamic-carbonic anhydride intermediates that in the presence of DMAP led to the final N-BOC product. The effect of N-methylimidazole in place of DMAP was also examined.

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