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1103-58-8

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1103-58-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1103-58-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,0 and 3 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1103-58:
(6*1)+(5*1)+(4*0)+(3*3)+(2*5)+(1*8)=38
38 % 10 = 8
So 1103-58-8 is a valid CAS Registry Number.
InChI:InChI=1/C20H24O7/c1-25-17-11-14(6-7-15(17)23)20(24)19(12-22)27-16-8-5-13(4-3-9-21)10-18(16)26-2/h3-8,10-11,19-24H,9,12H2,1-2H3/b4-3+

1103-58-8SDS

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 threo-1-(4-hydroxy-3-methoxyphenyl)-2-{4-[-(E)-3-hydroxy-1-propenyl]-2-methoxyphenoxy}-1,3-propanediol

1.2 Other means of identification

Product number -
Other names (+/-)-guaiacylglycerin-8-O-4'-coniferyl ether

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:1103-58-8 SDS

1103-58-8Downstream Products

1103-58-8Relevant articles and documents

Incorporation of catechyl monomers into lignins: Lignification from the non-phenolic end: Via Diels-Alder cycloaddition?

Ando, Daisuke,Boerjan, Wout,Elder, Thomas J.,Eugene, Alexis,Kim, Hoon,Lu, Fachuang,Ralph, John,Tobimatsu, Yuki,Vanholme, Ruben

, p. 8995 - 9013 (2021/11/27)

Canonical lignification occurs via the coupling of phenolic radicals, in which chain extension can occur only from phenolic ends of growing polymer chains. Radical coupling of catechyl monomers, including caffeyl and 5-hydroxyconiferyl alcohols, gives ris

On the reactivity of the Melanocarpus albomyces laccase and formation of coniferyl alcohol dehydropolymer (DHP) in the presence of ionic liquid 1-allyl-3-methylimidazolium chloride

Lahtinen, Maarit,Viikari, Liisa,Karhunen, Pirkko,Asikkala, Janne,Kruus, Kristiina,Kilpel?inen, Ilkka

, p. 169 - 177 (2013/01/15)

Some ionic liquids are able to dissolve wood, including lignin and lignocellulose, and thus they provide an efficient reaction media for modification of globally abundant wood-based polymers. Lignin can be modified with laccases (EC 1.10.3.2), multicopper

An enantiocomplementary dirigent protein for the enantioselective lacease-catalyzed oxidative coupling of phenols

Pickel, Benjamin,Constantin, Mihaela-Anca,Pfannstiel, Jens,Conrad, Juergen,Beifuss, Uwe,Schaller, Andreas

supporting information; experimental part, p. 202 - 204 (2010/03/30)

(+)- or (-)-plnoreslnol: that Is the question. Which of the two enantiomeric lignans is formed during laccasecatalyzed phenol coupling of (E)-coniferyl alcohol (1) depends on the dirigent protein. In the presence of the first enantiocomplementary dirigent protein AtDIR6, (-)-2 is formed (78 % ee). Preferential formation of (+)-2 is observed in the presence of the dirigent protein FiDIR1, whereas only racemic 2 is formed in the absence of dirigent proteins

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