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135716-08-4

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135716-08-4 Usage

General Description

Tert-butyl 4-(2-ethoxy-2-oxoethylidene)piperidine-1-carboxylate is a chemical compound with a complex structure consisting of a tert-butyl group attached to a piperidine ring. The piperidine ring is further functionalized with a carboxylate group and an ethoxyketene acetal group. This chemical compound has potential applications in the field of organic synthesis and drug discovery due to its unique structure and reactivity. It may be used as a building block in the synthesis of various pharmaceuticals and organic compounds, where its ethoxyketene acetal moiety can serve as a versatile protecting group for aldehydes and ketones, allowing for selective chemical transformations. Further research and experimentation are required to uncover the precise properties and applications of this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 135716-08-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,7,1 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 135716-08:
(8*1)+(7*3)+(6*5)+(5*7)+(4*1)+(3*6)+(2*0)+(1*8)=124
124 % 10 = 4
So 135716-08-4 is a valid CAS Registry Number.
InChI:InChI=1S/C14H23NO4/c1-5-18-12(16)10-11-6-8-15(9-7-11)13(17)19-14(2,3)4/h10H,5-9H2,1-4H3

135716-08-4SDS

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 4-(2-ethoxy-2-oxoethylidene)piperidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names tert-butyl 4-(2-ethoxy-2-oxoethylidene)tetrahydro-1(2H)-pyridinecarboxylate

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:135716-08-4 SDS

135716-08-4Relevant articles and documents

Substituted furo[3,2-b]pyridines: Novel bioisosteres of 5-HT1F receptor agonists

Mathes, Brian M.,Hudziak, Kevin J.,Schaus, John M.,Xu, Yao-Chang,Nelson, David L.,Wainscott, David B.,Nutter, Suzanne E.,Gough, Wendy H.,Branchek, Theresa A.,Zgombick, John M.,Filla, Sandra A.

, p. 167 - 170 (2004)

Synthesis and evaluation of a series of 2,3,5- and 3,5-substituted furo[3,2-b]pyridines were undertaken in order to investigate their utility as bioisosteres of 5-HT1F receptor agonist indole analogues, 1-3. The replacement proved to be effective, providing compounds with similar 5-HT 1F receptor affinity and improved selectivity when compared with the indole analogues. Through these studies we identified 4-fluoro-N-[3-(1-methyl- piperidin-4-yl)-furo[3,2-b]pyridin-5-yl]-benzamide (5), a potent and selective 5-HT1F receptor agonist with the potential to treat acute migraine.

Design, Synthesis, and Biological Evaluation of Novel Pyrimido[4,5-b]indole Derivatives against Gram-Negative Multidrug-Resistant Pathogens

Kong, Qidi,Pan, Wei,Xu, Heng,Xue, Yaru,Guo, Bin,Meng, Xin,Luo, Cheng,Wang, Ting,Zhang, Shuhua,Yang, Yushe

supporting information, p. 8644 - 8665 (2021/06/28)

Due to the poor permeability across Gram-negative bacterial membranes and the troublesome bacterial efflux mechanism, only a few GyrB/ParE inhibitors with potent activity against Gram-negative pathogens have been reported. Among them, pyrimido[4,5-b]indol

COMBINATIONS COMPRISING BENZODIOXOL AS GLP-1R AGONISTS FOR USE IN THE TREATMENT OF NASH/NAFLD AND RELATED DISEASES

-

Page/Page column 142; 143, (2020/12/07)

In part, the invention provides a new combination comprising (1) a GLP-1R agonist and (2) an ACC inhibitor or a DGAT2 inhibitor, or a KHK inhibitor or FXR agonist. The invention further provides new methods for treating diseases and disorders, for example, fatty liver, nonalcoholic fatty liver disease, nonalcoholic steatohepatitis, nonalcoholic steatohepatitis with liver fibrosis, nonalcoholic steatohepotitis with cirrhosis, and nonalcoholic steatohepatitis with cirrhosis and with hepatocellular carcinoma or with a metabolic-related disease, obesity, and type 2 diabetes, for example, using the new combination described herein.

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