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5-chloro-2-furfuryl alcohol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

27230-59-7

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27230-59-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27230-59-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,2,3 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 27230-59:
(7*2)+(6*7)+(5*2)+(4*3)+(3*0)+(2*5)+(1*9)=97
97 % 10 = 7
So 27230-59-7 is a valid CAS Registry Number.

27230-59-7SDS

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 (5-chlorofuran-2-yl)methanol

1.2 Other means of identification

Product number -
Other names 5-chloro-furfuryl alcohol

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:27230-59-7 SDS

27230-59-7Downstream Products

27230-59-7Relevant academic research and scientific papers

Visible-Light-Induced Intermolecular Dearomative Cyclization of Furans: Synthesis of 1-Oxaspiro[4.4]nona-3,6-dien-2-one

Dong, Wuheng,Yuan, Yao,Gao, Xiaoshuang,Keranmu, Miladili,Li, Wanfang,Xie, Xiaomin,Zhang, Zhaoguo

, p. 1461 - 1467 (2019/01/21)

A fac-Ir(ppy)3-catalyzed intermolecular dearomative cyclization of 2-bromo-2-((5-bromofuran-2-yl)methyl)malonate and alkynes affording substituted spirolactones in yields of 19-91% via a 5-exo-dig radical cyclization under visible light is presented. This method provides a new access to the synthesis of spirocycle skeletons applying water as an external oxygen source under mild reaction conditions.

Bifunctional Furfuryl Cations Strategy: Three-Component Synthesis of Enamidyl Triazoles

Yang, Hengtuo,Gou, Jing,Guo, Jiawei,Duan, Dongyu,Zhao, Yu-Ming,Yu, Binxun,Gao, Ziwei

supporting information, p. 129 - 133 (2016/01/25)

A new multicomponent synthesis of functionalized enamidyl triazoles starting from simple and readily available starting materials is described. A simple treatment of a dichloromethane solution of an azide, amine, and 5-bromo-2-furylcarbinol with a Lewis acid provides the enamidyl triazole in good to high yield. A triple domino sequence, formal [3+2] cycloaddition/ring-opening/amidation, is involved in this new skeleton-generating reaction.

Application of furyl-stabilized sulfur ylides to a concise synthesis of 8a-epi-swainsonine

Bi, Jie,Aggarwal, Varinder K.

, p. 120 - 122 (2008/09/19)

The total synthesis of 8a-epi-swainsonine has been achieved in 20% overall yield from R-glyceraldehyde dimethylacetonide 3 through epoxidation with the achiral furyl-substituted sulfonium ylide 2d as one of the key steps. The Royal Society of Chemistry.

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