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2-Nonen-4-ol, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

107200-33-9

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107200-33-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107200-33-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,2,0 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 107200-33:
(8*1)+(7*0)+(6*7)+(5*2)+(4*0)+(3*0)+(2*3)+(1*3)=69
69 % 10 = 9
So 107200-33-9 is a valid CAS Registry Number.

107200-33-9SDS

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 2-nonen-4-ol

1.2 Other means of identification

Product number -
Other names Non-2-en-4-ol

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:107200-33-9 SDS

107200-33-9Upstream product

107200-33-9Downstream Products

107200-33-9Relevant academic research and scientific papers

Tuning of α-Silyl Carbocation Reactivity into Enone Transposition: Application to the Synthesis of Peribysin D, E-Volkendousin, and E-Guggulsterone

Athawale, Paresh R.,Zade, Vishal M.,Rama Krishna, Gamidi,Reddy, D. Srinivasa

supporting information, p. 6642 - 6647 (2021/09/02)

A reliable method for enone transposition has been developed with the help of silyl group masking. Enantio-switching, substituent shuffling, and Z-selectivity are the highlights of the method. The developed method was applied for the first total synthesis of peribysin D along with its structural revision. Formal synthesis of E-guggulsterone and E-volkendousin was also claimed using a short sequence.

Synthesis with sulfones, Part XLIII. Preparation of γ-functionalized vinyl sulfones by nucleophilic substitution of allylidene disulfones; stereospecific reduction of 3-hydroxy-(E)-1-propenyl sulfones to (Z)-allylic alcohols

Cuvigny, T.,Penhoat, C. Herve du,Julia, M.

, p. 409 - 421 (2007/10/02)

The substitution of a sulfonyl moiety ao allylidene disulfones by various nucleophiles (PhSNa, PhSO2Na, H2O and R2NH) leads to γ-functionalized (E)-vinyl sulfones.The stereospecific reduction of 3-hydroxy-(E)-1-propenyl sulfones affords (Z)-allylic alcoho

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