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"3,7,13,17-tetrakis(carboxymethyl)-21H,23H-Porphine-2,8,12,18-tetrapropanoic acid" is a complex organic compound with a molecular formula of C40H40N4O8. It is a derivative of porphyrin, a large heterocyclic aromatic organic compound that is an essential component of hemoglobin, chlorophyll, and many other biological molecules. This specific compound features four carboxymethyl groups attached to the 3, 7, 13, and 17 positions of the porphyrin ring, and four propanoic acid groups attached to the 2, 8, 12, and 18 positions. The structure of 3,7,13,17-tetrakis(carboxymethyl)-21H,23H-Porphine-2,8,12,18-tetrapropanoic acid allows it to have potential applications in various fields, such as medicine, materials science, and catalysis, due to its unique chemical properties and ability to form complexes with metal ions.

531-42-0

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531-42-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 531-42-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,3 and 1 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 531-42:
(5*5)+(4*3)+(3*1)+(2*4)+(1*2)=50
50 % 10 = 0
So 531-42-0 is a valid CAS Registry Number.
InChI:InChI=1/C48H54N4O16/c1-61-40(53)14-9-25-26(10-15-41(54)62-2)33-22-37-31(20-46(59)67-7)28(12-17-43(56)64-4)35(51-37)24-39-47(48(60)68-8)29(13-18-44(57)65-5)36(52-39)23-38-30(19-45(58)66-6)27(11-16-42(55)63-3)34(50-38)21-32(25)49-33/h21-24,49,52H,9-20H2,1-8H3/b32-21-,33-22-,34-21-,35-24-,36-23-,37-22-,38-23-,39-24-

531-42-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3',3'',3'''-(3,7,13,17-tetrakis-carboxymethyl-21H,23H-porphine-2,8,12,18-tetrayl)-tetrakis-propionic acid

1.2 Other means of identification

Product number -
Other names -

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:531-42-0 SDS

531-42-0Downstream Products

531-42-0Relevant academic research and scientific papers

Non-enzymic tetramisation of ethyl 3-(4-ethoxycarbonylmethyl-1H-pyrrol-3-yl)propionate with formaldehyde follows a similar course to the non-enzymic tetramisation of porphobilinogen

Cheung, Kwai-Ming,Shoolingin-Jordan, Peter M.

, p. 5973 - 5976 (2007/10/03)

The octaethyl esters of uroporphyrins were formed directly from ethyl 3-(4-ethoxy-carbonylmethyl-1H-pyrrol-3-yl)propionate and formalin in a yield of ca. 30% with the isomers I, II, III and IV being formed in the ratio 1:1:4:2. Under anaerobic conditions, the colourless uroporphyrinogen esters were formed in a similar ratio. These observations parallel the non-enzymic formation of uroporphyrinogens from the naturally occurring tetrapyrrole precursor, porphobilinogen, highlighting the similarity in both tetramisation and isomerisation reactions.

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