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4-benzylmercapto-3-nitro-1,8-naphthalic anhydride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

625836-84-2

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625836-84-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 625836-84-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,5,8,3 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 625836-84:
(8*6)+(7*2)+(6*5)+(5*8)+(4*3)+(3*6)+(2*8)+(1*4)=182
182 % 10 = 2
So 625836-84-2 is a valid CAS Registry Number.

625836-84-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-benzylmercapto-3-nitro-1,8-naphthalic anhydride

1.2 Other means of identification

Product number -
Other names 4-(benzylthio)-3-nitro-1,8-naphthalic anhydride

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:625836-84-2 SDS

625836-84-2Relevant academic research and scientific papers

Synthesis of thiazo- or thiadiazo- naphthalene carboxamides via mercuric intermediates and their antitumor and DNA photocleavage activities

Li, Zhigang,Yang, Qing,Qian, Xuhong

, p. 6634 - 6641 (2005)

Two kinds of thiazo- or thiadiazo- naphthalene carboxamides with aminoalkyl side chains at 5- or 6-position modified from naphthalimides were designed, synthesized and quantitatively evaluated as antitumor and DNA photocleaving agents. The compound with a

Thiadiazole: A new family of intercalative photonuclease with electron transfer and radical mechanisms

Li, Yonggang,Xu, Yufang,Qian, Xuhong,Qu, Baoyuan

, p. 3513 - 3515 (2003)

A new family of photonuclease, thiadiazole-naphthalimide were synthesized and evaluated. Thiadiazole group was incorporated for the first time. These compounds intercalated into DNA efficiently and damaged DNA as low as 10 μM photochemically. Mechanism experiment showed that electron transfer and radicals were involved.

SULFUR-CONTAINING NAPHTHOYLIMIDE DERIVATIVES

-

Page/Page column 8, (2008/06/13)

The invention discloses novel sulfur-containing naphthalimide derivatives, and the preparation and uses thereof. The conjugated plane of naphthalimide derivatives of the invention is enlarged by incorporating 5-or 6-membered heteroaromatic ring and/or introducing S heteroatom, thus increasing the anti-tumor activity of naphthalimide. The compounds of the invention displays significant inhibiting activities to the proliferation of various tumor cells such as human lung cancer, gastric cancer, liver cancer, leucocythemia and the like. The inhibition of cell proliferation is dose-dependent.

Thio-heterocylic naphthalimides with aminoalkyl side chains: Novel alternative tools for photodegradation of genomic DNA without impairment on bioactivities of proteins

Yang, Qing,Qian, Xuhong,Xu, Jianqiang,Sun, Yuanshe,Li, Yonggang

, p. 1615 - 1622 (2007/10/03)

Thio-heterocylic naphthalimides (R1-R5) were designed, synthesized and evaluated as nonmetallic and long-wavelength photocleavers. Some of them showed highly efficient abilities in the degradation of plasmid and genomic DNA under the mild conditions witho

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