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Benzoyl chloride, 3-hydroxy-4-methoxy- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 289896-68-0 Structure
  • Basic information

    1. Product Name: Benzoyl chloride, 3-hydroxy-4-methoxy- (9CI)
    2. Synonyms: Benzoyl chloride, 3-hydroxy-4-methoxy- (9CI)
    3. CAS NO:289896-68-0
    4. Molecular Formula: C8H7ClO3
    5. Molecular Weight: 186.59238
    6. EINECS: N/A
    7. Product Categories: ACIDHALIDE
    8. Mol File: 289896-68-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 331.2±27.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.349±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 8.96±0.10(Predicted)
    10. CAS DataBase Reference: Benzoyl chloride, 3-hydroxy-4-methoxy- (9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: Benzoyl chloride, 3-hydroxy-4-methoxy- (9CI)(289896-68-0)
    12. EPA Substance Registry System: Benzoyl chloride, 3-hydroxy-4-methoxy- (9CI)(289896-68-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 289896-68-0(Hazardous Substances Data)

289896-68-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 289896-68-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,9,8,9 and 6 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 289896-68:
(8*2)+(7*8)+(6*9)+(5*8)+(4*9)+(3*6)+(2*6)+(1*8)=240
240 % 10 = 0
So 289896-68-0 is a valid CAS Registry Number.

289896-68-0SDS

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 3-hydroxy-4-methoxybenzoyl chloride

1.2 Other means of identification

Product number -
Other names 3-HYDROXY-4-METHOXY-BENZOYL CHLORIDE

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:289896-68-0 SDS

289896-68-0Upstream product

289896-68-0Relevant articles and documents

Total Synthesis and Biological Evaluation of Tiancimycins A and B, Yangpumicin A, and Related Anthraquinone-Fused Enediyne Antitumor Antibiotics

Aujay, Monette,Das, Dipendu,Gavrilyuk, Julia,Hammond, Mikhail,Lu, Yong,Lyssikatos, Joseph,Nicolaou, K. C.,Pitsinos, Emmanuel N.,Rout, Subhrajit,Sandoval, Joseph,Schammel, Alexander

supporting information, (2020/02/13)

The family of anthraquinone-fused enediyne antitumor antibiotics was established by the discovery of dynemicin A and deoxy-dynemicin A. It was then expanded, first by the isolation of uncialamycin, and then by the addition to the family of tiancimycins A-

Design, synthesis, and biological evaluation of novel tetrahydroisoquinoline derivatives as potential antitumor candidate

Zhu, Panhu,Ye, Wenfeng,Li, Jiaming,Zhang, Yanchun,Huang, Weijun,Cheng, Mohan,Wang, Yujun,Zhang, Yang,Liu, Huicai,Zuo, Jian

, p. 443 - 455 (2017/04/03)

A novel class of tetrahydroisoquinoline derivatives was designed and synthesized as antitumor agents and evaluated for their in vitro and in vivo biological activities. The antiproliferative activities of all the target compounds on HUVEC, MCF-7, and HT-2

Synthesis of aryl-substituted naphthalene-linked pyrrolobenzodiazepine conjugates as potential anticancer agents with apoptosis-inducing ability

Kamal, Ahmed,Reddy, M. Kashi,Ramaiah, M. Janaki,Srikanth,Rajender,Reddy, V. Santosh,Kumar, G. Bharath,Pushpavalli,Bag, Indira,Juvekar, Aarti,Sen, Subrata,Zingde, Surekha M.,Pal-Bhadra, Manika

experimental part, p. 1665 - 1679 (2012/01/05)

A library of new aryl-substituted naphthalene C8-linked pyrrolo[2,1-c][1,4]benzodiazepine (PBD) conjugates with various linker architectures were designed, synthesized, and evaluated for their anticancer activity against a panel of 11 human cancer cell lines. All 32 conjugates show anticancer potential, with some of them exhibiting particularly high activity (0.01-0.19μM). Thermal denaturation studies showed effective DNA binding capacity relative to DC-81. In assays for biological activity relating to cell-cycle distribution, these PBD conjugates induce G0/G1-phase arrest and also cause an increase in the levels of p53 and caspase-9 proteins, followed by apoptotic cell death. One conjugate in particular is the most promising candidate of the series, with the potential to be selected for further studies, either alone or in combination with existing anticancer therapies. Getting into the groove: Pyrrolobenzodiazepine (PBD) conjugates showed an effective ability to bind DNA. They induce G0/G1-phase arrest, enhance the expression levels of p53 and caspase-9, and induce apoptosis. One conjugate stands out as particularly promising; it is a suitable candidate for further study, either alone or in combination with current anticancer therapies.

NO-mediated aromatic nitration during decomposition of phenolic S-nitrosothiols in non-aqueous aerobic medium

Petit,Bernardes-Genisson,Hoffmann,Souchard,Labidalle

, p. 1634 - 1638 (2007/10/03)

Five novel S-nitrosothiol compounds (6-10) derived from L-cysteine were generated in solution and their decomposition rate was followed by UV spectroscopy. In acetonitrile, compounds 9 and 10 were the most stable of this series with a half-life of 24 h. T

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