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55583-11-4

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55583-11-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55583-11-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,5,8 and 3 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 55583-11:
(7*5)+(6*5)+(5*5)+(4*8)+(3*3)+(2*1)+(1*1)=134
134 % 10 = 4
So 55583-11-4 is a valid CAS Registry Number.

55583-11-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-bromo-2,4-bis(phenylmethoxy)benzene

1.2 Other means of identification

Product number -
Other names 2,4-dibenzyloxybromobenzene

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:55583-11-4 SDS

55583-11-4Relevant articles and documents

Synthesis of 2,6,9-substituted xanthen-3-one and solvent effect on structural and photophysical properties

Hisaeda, Yoshio,Iwamori, Shohei,Kawamata, Jun,Koga, Satoshi,Koide, Taro,Suzuki, Yasutaka

, (2020)

The synthesis of donor-π-donor type 2,6,9-substituted xanthen-3-one and its solvent effect on both the structural and photophysical properties were revealed. The keto-enol isomerization behavior and red-shift of the emission wavelengths were observed depe

A solution for detecting metal ion content of organic compound and use thereof

-

Paragraph 0067; 0199; 0200; 0201, (2017/09/26)

The invention relates to organic compounds used for detecting metal ion contents in solutions. The organic compounds can be used for biomedicine, environment monitoring, and the like. By introduction of color developing groups or fluorophores into ortho p

Enantioselective synthesis, stereochemical correction, and biological investigation of the rodgersinine family of 1,4-benzodioxane neolignans

Pilkington, Lisa I.,Barker, David,Wagoner, Jessica,Polyak, Stephen J.

supporting information, p. 1046 - 1049 (2015/03/30)

The enantioselective synthesis and chiroptic analysis of all members of the rodgersinine family of 1,4-benzodioxane neolignans has been achieved. ECD spectra and optical rotation analysis determined that the previously published stereochemistry of trans-rodgersinines A and B was incorrect. The cis-rodgersinines A and B did not follow the model ECD study commonly used to assign the absolute stereochemistry of 1,4-benzodioxane natural products. This finding has implications on the absolute stereochemistry of other natural products of this type. Additionally, the rodgersinines were found to have anti-HCV activities.

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