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151071-02-2

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151071-02-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 151071-02-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,0,7 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 151071-02:
(8*1)+(7*5)+(6*1)+(5*0)+(4*7)+(3*1)+(2*0)+(1*2)=82
82 % 10 = 2
So 151071-02-2 is a valid CAS Registry Number.

151071-02-2SDS

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 methyl (E)-3-[4-(acetyloxy)-3-(3-methyl-2-butenyl)phenyl]-2-propenoate

1.2 Other means of identification

Product number -
Other names methyl-3-prenyl-4-acetoxycinnamate

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:151071-02-2 SDS

151071-02-2Relevant articles and documents

Artepillin C isoprenomics: Design and synthesis of artepillin C isoprene analogues as lipid peroxidation inhibitor having low mitochondrial toxicity

Uto, Yoshihiro,Ae, Shutaro,Koyama, Daisuke,Sakakibara, Mitsutoshi,Otomo, Naoki,Otsuki, Mamoru,Nagasawa, Hideko,Kirk, Kenneth L.,Hori, Hitoshi

, p. 5721 - 5728 (2007/10/03)

We designed and synthesized isoprene analogues of artepillin C, a major component of Brazilian propolis, and investigated the inhibitory activity on lipid peroxidation of rat liver mitochondria (RLM) and RLM toxicity based on isoprenomics. We succeeded in

The synthesis of Plicatin B via the Heck reaction

Bates,Gabel

, p. 3547 - 3550 (2007/10/02)

The anti-microbial natural product Plicatin B has been synthesized in 53% overall yield using a Heck reaction as the key step. The optimum conditions for this reaction have been determined. Halophenols proved much less reactive than their corresponding ac

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