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3-Cyclohexen-1-one, 2,2,4-trimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87128-98-1

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87128-98-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87128-98-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,1,2 and 8 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 87128-98:
(7*8)+(6*7)+(5*1)+(4*2)+(3*8)+(2*9)+(1*8)=161
161 % 10 = 1
So 87128-98-1 is a valid CAS Registry Number.

87128-98-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,4-trimethyl-3-cyclohexen-1-one

1.2 Other means of identification

Product number -
Other names 2,2,4-Trimethyl-3-cyclohexen-1-one

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:87128-98-1 SDS

87128-98-1Relevant academic research and scientific papers

Synthesis of paclitaxel. 1. synthesis of the abc ring of paclitaxel by SmI2-mediated cyclization

Fukaya, Keisuke,Tanaka, Yuta,Sato, Ayako C.,Kodama, Keisuke,Yamazaki, Hirohisa,Ishimoto, Takeru,Nozaki, Yasuyoshi,Iwaki, Yuki M.,Yuki, Yohei,Umei, Kentaro,Sugai, Tomoya,Yamaguchi, Yu,Watanabe, Ami,Oishi, Takeshi,Sato, Takaaki,Chida, Noritaka

, p. 2570 - 2573 (2015/06/16)

A convergent synthesis of the ABC ring of antitumor natural product paclitaxel (Taxol) is described. SmI2-mediated reductive cyclization of an allylic benzoate possessing an aldehyde function, synthesized from tri-O-acetyl-d-glucal and 1,3-cyclohexanedione, smoothly afforded the highly strained 6-8-6 tricarbocyclic structure in 66% yield.

Glycinoeclepins, Natural Hatching Stimuli for the Soybean Cyst Nematode, Heterodera Glycines. II. Structural Elucidation

Masamune, Tadashi,Fukuzawa, Akio,Furusaki, Akio,Ikura, Mitsuhiko,Matsue, Hideki,et al.

, p. 1001 - 1014 (2007/10/02)

The structures of three new compounds, glycinoeclepsins A, B, and C, isolated from the hatch-stimulating extracts of kidney beans for the soybean cyst nematode, have been determined.The structures were resolved by using spectroscopic methods, especially b

Preparation of 2-exo-Hydroxy-7-oxabicyclo[2.2.1]heptanes

-

, (2008/06/13)

2-exo-Hydroxy-7-oxabicyclo[2.2.1]heptanes are prepared by treating the corresponding cis-epoxycyclohexanol with acid in an inert solvent or by treating a 3-cyclohexen-1-ol which will produce the corresponding cis-epoxy alcohol successively or concurrently with an oxidizing agent and an acid in an inert solvent.

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