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3284-47-7

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3284-47-7 Usage

Synthesis Reference(s)

Journal of Heterocyclic Chemistry, 28, p. 1671, 1991 DOI: 10.1002/jhet.5570280705Tetrahedron Letters, 3, p. 921, 1962

Check Digit Verification of cas no

The CAS Registry Mumber 3284-47-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,8 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3284-47:
(6*3)+(5*2)+(4*8)+(3*4)+(2*4)+(1*7)=87
87 % 10 = 7
So 3284-47-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H11NO2/c1-3-11-8(10)7-6(2)4-5-9-7/h4-5,9H,3H2,1-2H3

3284-47-7SDS

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 Ethyl 3-methyl-1H-pyrrole-2-carboxylate

1.2 Other means of identification

Product number -
Other names 3-Methyl-2,4-dithiouracil

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:3284-47-7 SDS

3284-47-7Relevant articles and documents

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Corwin,Straughn

, p. 2968 (1948)

-

DBU-promoted tandem Michael-addition/cyclization for the synthesis of polysubstituted pyrroles

Yang, Tianyu,Wang, Ke-Hu,Huang, Danfeng,Li, Pengfei,Deng, Zhoubin,Su, Yinpeng,Hu, Yulai

, p. 2291 - 2297 (2019/03/06)

An efficient and transition-metal-free method for the synthesis of the structurally diversified pyrroles is described. Various α,β-unsaturated ynones reacted with N-substituted ethyl glycine ethyl ester hydrochlorides in the presence of DBU to form the co

HETEROCYCLIC INHIBITORS OF NECROPTOSIS

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Page/Page column 36, (2009/04/25)

The invention features a series of heterocyclic derivatives that inhibit tumor necrosis factor alpha (TNF-α) induced necroptosis. The heterocyclic compounds of the invention are described by Formulas (I) and (Ia)-(Ie) and are shown to inhibit TNF-α induce

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