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129724-80-7

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129724-80-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129724-80-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,7,2 and 4 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 129724-80:
(8*1)+(7*2)+(6*9)+(5*7)+(4*2)+(3*4)+(2*8)+(1*0)=147
147 % 10 = 7
So 129724-80-7 is a valid CAS Registry Number.

129724-80-7SDS

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 (3R)-5-O-acetyl-1-[(S)-phenylethyl]-mevalonamide

1.2 Other means of identification

Product number -
Other names (3R)-5-O-acetyl-1-[(1S)-1-phenylethyl]mevalonamide

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:129724-80-7 SDS

129724-80-7Downstream Products

129724-80-7Relevant articles and documents

Anti-inflammatory lanostane-type triterpene acids from Piptoporus betulinus

Kamo, Tsunashi,Asanoma, Masashi,Shibata, Hisao,Hirota, Mitsuru

, p. 1104 - 1106 (2003)

Six lanostane-type triterpene acids were isolated from the fruiting bodies of Piptoporus betulinus. They were identified as polyporenic acids A (1) and C (2), three derivatives of polyporenic acid A (3-5), and a novel compound, (+)-12α, 28-dihydroxy-3α-(3

Revised chirality of the acyl group of 8′-O-(3-hydroxy-3- methylglutaryl)-8′-hydroxyabscisic acid

Kamo, Tsunashi,Hirai, Nobuhiro,Matsumoto, Chiaki,Ohigashi, Hajime,Hirota, Mitsuru

, p. 2517 - 2520 (2004)

The chirality of the acyl group 8′-O-(3-Hydroxy-3-methylglutaryl)- 8′-hydroxyabscisic acid was revised to S based on an HPLC analysis of the diastereomer derived from mevalonolactone obtained by reduction of the conjugate with lithium borohydride. 8′-O-(3

Flavonoids and a Limonoid from the Fruits of Citrus unshiu and Their Biological Activity

Eom, Hee Jeong,Lee, Dahae,Lee, Seulah,Noh, Hyung Jun,Hyun, Jae Wook,Yi, Pyoung Ho,Kang, Ki Sung,Kim, Ki Hyun

, p. 7171 - 7178 (2016)

The fruits of Citrus unshiu are one of the most popular and most enjoyed fruits in Korea. As we continue to seek for bioactive metabolites from Korean natural resources, our study on the chemical constituents of the fruits of C. unshiu resulted in the isolation of a new flavonoid glycoside, limocitrunshin 1, along with seven other flavonoids 2-8 and a limonoid 9. All structures were identified by spectroscopic methods, namely 1D and 2D NMR, including HSQC, HMBC, and 1H-1H COSY experiments, HRMS, and other chemical methods. Compounds 3, 5, and 9 are reported to be isolated from this fruit for the first time. The isolated compounds were applied to activity tests to verify their inhibitory effects on inflammation and nephrotoxicity. Compounds 6 and 9 showed the most potent inhibitory activity on renal cell damage and nitric oxide production, respectively. Thus, the fruits of C. unshiu could serve as a valuable natural source of bioactive components with health benefits for potential application in functional foods.

Eudesmane Glycosides from Ambrosia artemisiifolia (Common Ragweed) as Potential Neuroprotective Agents

An, Jin-Pyo,Ha, Thi Kim Quy,Kim, Hyun Woo,Ryu, Byeol,Kim, Jinwoong,Park, Junsoo,Lee, Chul Ho,Oh, Won Keun

, p. 1128 - 1138 (2019)

In Alzheimer's disease, amyloid-β (Aβ) accumulation in the brain results in neuronal cell death and is one of the major causes of dementia. Because the current therapeutic agents are not yet sufficiently effective or safe, there have been attempts to find

C-Methylated flavanones from the rhizomes of Matteuccia intermedia and their α-glucosidase inhibitory activity

Li, Xue,Zhu, Ling-Juan,Chen, Jin-Peng,Shi, Chen-Yu,Niu, Li-Ting,Zhang, Xue,Yao, Xin-Sheng

, (2019/05/17)

One new flavanonol, demethylmatteucinol (1), and nine new flavanone glucoside derivatives, matteflavosides H-J (2–4) and matteuinterates A-F (5–10), were isolated from the rhizomes of Matteuccia intermedia C.Chr., along with 21 known flavanones (11?31). N

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