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80638-49-9

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80638-49-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80638-49-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,6,3 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 80638-49:
(7*8)+(6*0)+(5*6)+(4*3)+(3*8)+(2*4)+(1*9)=139
139 % 10 = 9
So 80638-49-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H14O4/c1-14-9-6-8(4-3-5-12)7-10(15-2)11(9)13/h5-7,13H,3-4H2,1-2H3

80638-49-9SDS

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-(4-hydroxy-3,5-dimethoxyphenyl)propanal

1.2 Other means of identification

Product number -
Other names Propanal,3-(4-hydroxy-3,5-dimethoxyphenyl)

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:80638-49-9 SDS

80638-49-9Downstream Products

80638-49-9Relevant articles and documents

A single amino acid determines the catalytic efficiency of two alkenal double bond reductases produced by the liverwort Plagiochasma appendiculatum

Wu, Yifeng,Cai, Yuanheng,Sun, Yi,Xu, Ruixue,Yu, Haina,Han, Xiaojuan,Lou, Hongxiang,Cheng, Aixia

, p. 3122 - 3128 (2013/09/23)

Alkenal double bond reductases (DBRs) catalyze the NADPH-dependent reduction of the α,β-unsaturated double bond of many secondary metabolites. Two alkenal double bond reductase genes PaDBR1 and PaDBR2 were isolated from the liverwort species Plagiochasma appendiculatum. Recombinant PaDBR2 protein had a higher catalytic activity than PaDBR1 with respect to the reduction of the double bond present in hydroxycinnamyl aldehydes. The residue at position 56 appeared to be responsible for this difference in enzyme activity. The functionality of a C56 to Y56 mutation in PaDBR1 was similar to that of PaDBR2. Further site-directed mutagenesis and structural modeling suggested that the phenol ring stacking between this residue and the substrate was an important determinant of catalytic efficiency.

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