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3070-87-9

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3070-87-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3070-87-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,7 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3070-87:
(6*3)+(5*0)+(4*7)+(3*0)+(2*8)+(1*7)=69
69 % 10 = 9
So 3070-87-9 is a valid CAS Registry Number.

3070-87-9SDS

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 2',2'''-Dinitro-4',4'''-oxybisacetanilide

1.2 Other means of identification

Product number -
Other names N-[4-(4-acetylamino-3-nitrophenoxy)-2-nitrophenyl]acetamide

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:3070-87-9 SDS

3070-87-9Relevant articles and documents

Preparation method 3,3 '-dinitro -4, 4' - diacetyl diaminodiphenyl ether

-

Paragraph 0069; 0071-0073; 0075-0077; 0079-0081; 0084; ..., (2021/09/26)

The preparation method of 3, 3 ’ -dinitro -4 and 4 ’ -diacetyl diaminodiphenyl ether comprises the following steps of: adding an acylating agent to 4 and 4 ’ - diaminodiphenyl ether to carry out acylation reaction to obtain an acylation product. The nitra

Newly synthesized bis-benzimidazole derivatives exerting anti-tumor activity through induction of apoptosis and autophagy

Wang, Xiu-Jun,Chu, Na-Ying,Wang, Qin-He,Liu, Chao,Jiang, Chun-Guo,Wang, Xiao-Yu,Ikejima, Takashi,Cheng, Mao-Sheng

supporting information, p. 6297 - 6300 (2012/11/06)

In this study, a new series of bis-benzimidazole derivatives were designed and synthesized. Most of these new compounds showed significant anti-tumor activity in vitro compared to Hoechst 33258. Among them, the most potent compound 8 had the IC50/su

Synthesis and structure of Di[methoxy(ethoxy)carbonylamino-1H-benzimidazol- 5-yl] ethers

Pilyugin,Sapozhnikov,Kiseleva,Sapozhnikova,Vorob'eva,Klimakova

, p. 1509 - 1513 (2007/10/03)

A procedure was developed for preparing di[methoxy(ethoxy)carbonylamino-1H- benzimidazol-5-yl] ethers by the reaction of methyl or ethyl chloroformate with sodium cyanamide, followed by the reaction of the resulting methyl or ethyl cyanocarbamate with 4-(3,4-diaminophenoxy)-1,2-phenylenediamine in acidic solution. 2005 Pleiades Publishing, Inc.

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