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65866-00-4

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65866-00-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65866-00-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,8,6 and 6 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 65866-00:
(7*6)+(6*5)+(5*8)+(4*6)+(3*6)+(2*0)+(1*0)=154
154 % 10 = 4
So 65866-00-4 is a valid CAS Registry Number.

65866-00-4SDS

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 Methyl (2E)-4-(triphenylphosphoranylidene)-2-butenoate

1.2 Other means of identification

Product number -
Other names 2-Buten-1-ol,3-methoxy-,(2E)

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:65866-00-4 SDS

65866-00-4Relevant articles and documents

KM-01, a brassinolide inhibitor, its production, isolation and structure from two fungi Drechslera avenae and Pycnoporus coccineus

Kim, Seong-Kie,Hatori, Makoto,Ojika, Makoto,Sakagami, Youji,Marumo, Shingo

, p. 1975 - 1982 (1998)

A new brassinolide inhibitor, named KM-01, was isolated from the culture filtrates of two fungal species, Drechslera avenae and Pycnoporus coccineus, and the structure with absolute stereochemistry was elucidated as the fatty acid ester of an eremophilane sesquiterpene, bipolaroxin, based on spectroscopic analysis, chemical degradation, and synthesis of the fatty acid. Copyright (C) 1998 Elsevier Science Ltd.

Fast and efficient one step synthesis of dienamides

Mathieson, Jennifer E.,Crawford, James J.,Schmidtmann, Marc,Marquez, Rodolfo

experimental part, p. 2170 - 2175 (2009/09/04)

A fast and efficient one-step approach to the synthesis of dienamides is reported. This concise methodology relies on the use of imides as reactive intermediates and allows for the preferential formation of Z,E-dienamides in good yields.

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