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2973-77-5

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2973-77-5 Usage

Chemical Properties

pink to pale brown crystalline powder or needles

Uses

3,5-Dibromo-4-hydroxybenzaldehyde is a marine antibiotic derived from marine bacteria (organism).

Check Digit Verification of cas no

The CAS Registry Mumber 2973-77-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,7 and 3 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2973-77:
(6*2)+(5*9)+(4*7)+(3*3)+(2*7)+(1*7)=115
115 % 10 = 5
So 2973-77-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H4Br2O2/c8-5-1-4(3-10)2-6(9)7(5)11/h1-3,11H

2973-77-5 Well-known Company Product Price

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  • Alfa Aesar

  • (A12780)  3,5-Dibromo-4-hydroxybenzaldehyde, 98%   

  • 2973-77-5

  • 5g

  • 266.0CNY

  • Detail
  • Alfa Aesar

  • (A12780)  3,5-Dibromo-4-hydroxybenzaldehyde, 98%   

  • 2973-77-5

  • 25g

  • 1249.0CNY

  • Detail
  • Alfa Aesar

  • (A12780)  3,5-Dibromo-4-hydroxybenzaldehyde, 98%   

  • 2973-77-5

  • 100g

  • 4118.0CNY

  • Detail

2973-77-5SDS

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 3,5-Dibromo-4-hydroxybenzaldehyde

1.2 Other means of identification

Product number -
Other names 4-hydroxy-3,5-dibromobenzaldehyde

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:2973-77-5 SDS

2973-77-5Relevant articles and documents

Efficient and convenient synthesis of 3,4,5-trimethoxybenzaldehyde from p-cresol

Ji, Ya-Fei,Zong, Zhi-Min,Wei, Xian-Yong

, p. 2809 - 2814 (2002)

With p-cresol as starting material, 3,4,5-trimethoxybenzaldehyde was synthesized in an overall yield of 67.4% via bromination, hydrolysis, methoxylation and methylation.

Magnetic nano-structured cobalt-cobalt oxide/nitrogen-doped carbon material as an efficient catalyst for aerobic oxidation of p-cresols

Liang, Cheng,Li, Xuefeng,Su, Diefeng,Ma, Qiyi,Mao, Jianyong,Chen, Zhirong,Wang, Yong,Yao, Jia,Li, Haoran

, p. 121 - 131 (2018/05/22)

Efficient aerobic oxidation has been developed for the selective preparation of a sequence of valuable p-hydroxybenzaldehydes from corresponding p-cresols, using a new magnetically separable catalyst of nano-structured cobalt-cobalt oxide/nitrogen-doped carbon (CoOx@CN) material. CoOx@CN showed high activity for the 2-methoxy-4-cresol oxidation to vanillin, giving great yield (90%) and with good turnover number (210), as well as other p-cresols in good to great yields. The catalytic performance was investigated and related to the structural, chemical and magnetic properties which determined by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Fourier-transform infrared spectroscopy (FT-IR) and vibrating sample magnetometer (VSM). The effects of base to substrate molar ratio, catalyst concentration, temperature, and solvent on the conversion and selectivity patterns also have been studied. The investigation revealed that remarkable catalytic properties of CoOx@CN could be ascribed to the active species cobalt oxide, doped nitrogen and porous carbon with large surface area. The size of the catalyst is a key factor for catalyst performance. The ferromagnetic property of catalyst enables to recycle easily by an external magnetic field and reuse six successive times without significant activity loss.

A short and efficient total synthesis of the bromotyrosine-derived alkaloid psammaplysene A

Xu, Jingjing,Wang, Kai,Wu, Jinlong

, p. 13747 - 13749 (2018/04/25)

Psammaplysene A, an inhibitor of FOXO1a-mediated nuclear export, has been synthesized by a concise and improved route from tyrosine-derived acid and amine fragments which were easily constructed using commercially available p-hydroxybenzaldehyde and tyramine as starting material, respectively. The strategy provides an efficient access of psammaplysene analogues that can be explored for potential pharmaceutical or biological activities.

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