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54915-68-3

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54915-68-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54915-68-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,9,1 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 54915-68:
(7*5)+(6*4)+(5*9)+(4*1)+(3*5)+(2*6)+(1*8)=143
143 % 10 = 3
So 54915-68-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H15NO2/c1-2-15-12(14)13-9-5-7-10-6-3-4-8-11(10)13/h3-4,6,8H,2,5,7,9H2,1H3

54915-68-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-dihydro-2H-quinolin-1-carboxylic acid ethyl ester

1.2 Other means of identification

Product number -
Other names 1-Ethoxycarbonyl-1,2,3,4-tetrahydroquinoline

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:54915-68-3 SDS

54915-68-3Relevant articles and documents

Nickel-mediated inter- and intramolecular reductive cross-coupling of unactivated alkyl bromides and aryl iodides at room temperature

Yan, Chang-Song,Peng, Yu,Xu, Xiao-Bo,Wang, Ya-Wen

, p. 6039 - 6048 (2012/06/18)

A nickel-mediated intermolecular reductive cross-coupling reaction of unactivated alkyl bromides and aryl iodides at room temperature has been developed and successfully extended to less explored intramolecular versions and tandem cyclization-intermolecular cross-coupling. Highly stereoselective (or stereospecific) synthesis of linear-fused perhydrofuro[2,3-b]furan (pyran) and spiroketal skeletons allows rapid access to these useful building blocks, which would be potentially valuable in the synthesis of relevant natural products. A rational explanation for the formation of contiguous stereogenic centers is given. Copyright

SMALL MOLECULE MODIFIERS OF MICRORNA MIR-122

-

Page/Page column 38; 41, (2011/08/08)

MicroRNAs are a class of endogenous regulators of gene function. Aberrant regulation of microRNAs has been linked to various human diseases, most importantly cancer. Small molecule intervention of microRNA misregulation has the potential to provide new th

A facile one-pot synthesis of N-substituted tetrahydroquinolines

Babu, Thelagathoti Hari,Shanthi, Gnanamani,Perumal, Paramasivan T.

experimental part, p. 2881 - 2884 (2009/09/06)

An uncatalyzed one-pot synthesis of N-substituted tetrahydroquinolines was achieved in good yields by the reaction of quinoline and alkyl/acyl halides with Hantzsch dihydropyridine ester under mild reaction conditions.

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