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20041-39-8

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20041-39-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20041-39-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,0,4 and 1 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 20041-39:
(7*2)+(6*0)+(5*0)+(4*4)+(3*1)+(2*3)+(1*9)=48
48 % 10 = 8
So 20041-39-8 is a valid CAS Registry Number.
InChI:InChI=1/C16H25NO3/c1-5-6-13-7-8-15(16(9-13)19-4)20-11-14(18)10-17-12(2)3/h5,7-9,12,14,17-18H,1,6,10-11H2,2-4H3

20041-39-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-methoxy-4-prop-2-enylphenoxy)-3-(propan-2-ylamino)propan-2-ol

1.2 Other means of identification

Product number -
Other names 1-Isopropylamino-3-eugenoxypropanol-2

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:20041-39-8 SDS

20041-39-8Downstream Products

20041-39-8Relevant articles and documents

A new aspect of view in synthesizing new type β-adrenoceptor blockers with ancillary antioxidant activities

Huang, Yeun-Chih,Wu, Bin-Nan,Yeh, Jwu-Lai,Chen, Sheue-Jiun,Liang, Jyh-Chong,Lo, Yi-Ching,Chen, Ing-Jun

, p. 1739 - 1746 (2007/10/03)

A series of vanilloid-type β-adrenoceptor blockers derived from traditional Chinese herbal medicines were synthesized and tested for their antioxidant and adrenoceptor antagonistic activities. They all possessed significant β-adrenoceptor blocking activities under in vitro experiments and radioligand binding assays. In addition, some compounds were further examined in in vito tests and produced antagonist effects matching that of propranolol and labetalol by measurements of antagonism toward (-)isoproterenol-induced tachycardia and (-)phenylephrine-induced pressor responses in anesthetized rats. Furthermore, all of the compounds had antioxidant effects inherited from their original structures. In conclusion, compound 11 had the most potent β-adrenoceptors blocking activity, 12 and 13 possessed high cardioselectivity, whereas 14, 15 and 16 possessed additional α-adrenoceptor blocking activity and 15 is the most effective antioxidant of all. the antioxidant activity may be due to their @α and β unsaturated side chain at position 1 and ortho-substituted methoxy moiety on 4-phenoxyethylamine. Copyright

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