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61010-01-3

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61010-01-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61010-01-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,0,1 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 61010-01:
(7*6)+(6*1)+(5*0)+(4*1)+(3*0)+(2*0)+(1*1)=53
53 % 10 = 3
So 61010-01-3 is a valid CAS Registry Number.
InChI:InChI=1/C50H43O2.ClHO4/c1-5-18-37(19-6-1)45-33-47(39-22-9-3-10-23-39)51-49-41(26-14-28-43(45)49)31-35-16-13-17-36(30-35)32-42-27-15-29-44-46(38-20-7-2-8-21-38)34-48(52-50(42)44)40-24-11-4-12-25-40;2-1(3,4)5/h1-12,18-25,30-34H,13-17,26-29H2;(H,2,3,4,5)/q+1;/p-1

61010-01-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-[(E)-[3-[(E)-(2,4-diphenyl-6,7-dihydro-5H-chromen-1-ium-8-ylidene)methyl]cyclohex-2-en-1-ylidene]methyl]-2,4-diphenyl-6,7-dihydro-5H-chromene,perchlorate

1.2 Other means of identification

Product number -
Other names 8-[(E)-[3-[(E)-(2,4-diphenyl-6,7-dihydro-5H-chromen-1-ium-8-ylidene)methyl]cyclohex-2-en-1-ylidene]methyl]-2,4-diphenyl-6,7-dihydro-5H-chromene perchlorate

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:61010-01-3 SDS

61010-01-3Downstream Products

61010-01-3Relevant articles and documents

A near-infrared light-emitting organic material of the preparation method

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Paragraph 0025; 0026; 0027; 0028; 0029, (2017/05/10)

The invention discloses a preparation method of a novel near-infrared organic luminescent material, which comprises the following steps: A. stirring 2-methyl cyclohexanone or cyclohexanone or cyclopentanone, chalcone, solid potassium hydroxide and benzyltriethylammonium chloride at room temperature to obtain a compound disclosed as chemical general formula 4; B. mixing the compound disclosed as chemical general formula 4 with R1-CHO to prepare a compound disclosed as chemical general formula 6, or mixing a compound 4a with 5 times of 1,4-dihydro-2,6-dimethoxybenzene to obtain a compound 5. After the compound is recrystallized and purified, the yield is greater than 80% and is much higher than the yield in the document. The method has the advantages of reasonable technological design and high yield, and is economical and feasible.

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