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219144-65-7

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219144-65-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 219144-65-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,9,1,4 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 219144-65:
(8*2)+(7*1)+(6*9)+(5*1)+(4*4)+(3*4)+(2*6)+(1*5)=127
127 % 10 = 7
So 219144-65-7 is a valid CAS Registry Number.

219144-65-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,4,5-tetramethoxy-3-tridecylbenzene

1.2 Other means of identification

Product number -
Other names 1-(2,3,5,6-tetramethoxyphenyl)-tridecane

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:219144-65-7 SDS

219144-65-7Relevant articles and documents

Design, synthesis and α-glucosidase inhibition study of novel embelin derivatives

Chen, Wenhua,Chen, Xiaole,Gao, Min,Hong, Weiqian David,Jian, Rongchao,Li, Yuling,Sheng, Zhaojun,Tang, Xiaowen,Wu, Panpan,Zhang, Kun,Zhao, Denggao,Zheng, Xi

, p. 565 - 573 (2020/02/15)

Embelin is a naturally occurring para-benzoquinone isolated from Embelia ribes (Burm. f.) of the Myrsinaceae family. It was first discovered to have potent inhibitory activity (IC50 = 4.2 μM) against α-glucosidase in this study. Then, four seri

MULTIFUNCTIONAL RADICAL QUENCHERS

-

, (2014/05/07)

The invention provides a compound of formula (I): [insert formula (I)] wherein X, Y, and R1-R4 have any of the values defined in the specification, and salts thereof, as well as compositions comprising the compounds or salts. The compounds are useful for treating diseases associated with impaired mitochondrial function in an animal.

Total synthesis of maesanin and analogues

Poigny, Stephane,Guyot, Michele,Samadi, Mohammad

, p. 14791 - 14802 (2007/10/03)

An efficient total synthesis of maesanin and related quinones is reported, through direct alkylation of 1,2,4,5-tetramethoxybenzene with alkylbromides, followed by oxidation with ceric ammonium nitrate (CAN) which provokes formation of the quinone and dep

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