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3,5-dimethyl-1H-pyrrole-2,4-dicarbohydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87781-09-7

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87781-09-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87781-09-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,7,8 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 87781-09:
(7*8)+(6*7)+(5*7)+(4*8)+(3*1)+(2*0)+(1*9)=177
177 % 10 = 7
So 87781-09-7 is a valid CAS Registry Number.

87781-09-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-dimethyl-1H-pyrrole-2,4-dicarbohydrazide

1.2 Other means of identification

Product number -
Other names 3,5-Dimethyl-pyrrol-2,4-dicarbonsaeure-dihydrazid

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:87781-09-7 SDS

87781-09-7Downstream Products

87781-09-7Relevant articles and documents

Bis-isatin hydrazones with novel linkers: Synthesis and biological evaluation as cytotoxic agents

Ibrahim, Hany S.,Abou-Seri, Sahar M.,Ismail, Nasser S.M.,Elaasser, Mahmoud M.,Aly, Mohamed H.,Abdel-Aziz, Hatem A.

, p. 415 - 422 (2015/12/24)

Many bis-isatins and isatins with hydrazide extension were reported to have a potential anti-proliferative effects against different cancer cell lines and cancer targets. In this study, four series of bis-isatins with hydrazide linkers were synthesized. These compounds were investigated for their antitumor activity by assessing their cytotoxic potency against HepG2, MCF-7 and HCT-116 cancer cell lines. Compound 21c possessed significant cytotoxic activity against MCF-7 (IC50 = 1.84 μM) and HCT-116 (IC50 = 3.31 μM) that surpasses the activity of doxorubicin against both cell lines (MCF-7; IC50 = 2.57 μM and HCT-116; IC50 = 3.70 μM). Cell cycle analysis and annexin V-FITC staining of MCF-7 cells treated with 21c suggested that the cytotoxic effect of the compound could be attributed to its pro-apoptotic activity.

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