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211935-29-4

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211935-29-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 211935-29-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,1,9,3 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 211935-29:
(8*2)+(7*1)+(6*1)+(5*9)+(4*3)+(3*5)+(2*2)+(1*9)=114
114 % 10 = 4
So 211935-29-4 is a valid CAS Registry Number.

211935-29-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name O-benzyl-eugenol

1.2 Other means of identification

Product number -
Other names 2-Benzyloxy-1-methoxy-3-(prop-2-enyl)benzene

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:211935-29-4 SDS

211935-29-4Downstream Products

211935-29-4Relevant articles and documents

Highly convergent total synthesis of (+)-lithospermic acid via a late-stage intermolecular C-H olefination

Wang, Dong-Hui,Yu, Jin-Quan

supporting information; experimental part, p. 5767 - 5769 (2011/06/22)

The total synthesis of (+)-lithospermic acid is reported, which exploits two successive C-H activation reactions as key steps. Rh-catalyzed carbene C-H insertion reaction utilizing Davies's catalyst was used to forge dihydrobenzofuran core, and a late-sta

DIHYDROBENZOFURANYL ALKANAMINE DERIVATIVES AS 5HT2C AGONISTS

-

Page/Page column 57-58, (2008/06/13)

Compounds of Formula (I) or pharmaceutically acceptable salts thereof are provided: Formula (I) which are agonists or partial agonists of the 2C subtype of brain serotonin receptors. The compounds, and compositions containing the compounds, can be used to treat a variety of central nervous system disorders such as schizophrenia.

Synthesis of the bisbenzannelated spiroketal core of the γ-rubromycins. The use of a novel Nef-type reaction mediated by Pearlman's catalyst

Capecchi, Tanya,De Koning, Charles B.,Michael, Joseph P.

, p. 2681 - 2688 (2007/10/03)

The synthesis of the bisbenzannelated spiroketal core 6 of γ-rubromycin 1 from the substituted nitrostyrene 20 was achieved by using a novel Nef-type reaction mediated by Pearlman's catalyst. The precursor 28 was synthesised from readily prepared starting materials using Henry condensation chemistry. The product 6 was found to exist in two conformations in solution as shown by NMR spectroscopy.

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