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6954-16-1

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6954-16-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6954-16-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,5 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6954-16:
(6*6)+(5*9)+(4*5)+(3*4)+(2*1)+(1*6)=121
121 % 10 = 1
So 6954-16-1 is a valid CAS Registry Number.

6954-16-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-chloro-1,4-dioxaspiro[4.5]decane

1.2 Other means of identification

Product number -
Other names 6-Chlor-1,4-dioxa-spiro[4.5]decan

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:6954-16-1 SDS

6954-16-1Relevant articles and documents

One-step for the preparation of α-haloacetal of ketones with N-bromosuccinimide/N-chlorosuccinimide (NBS/NCS) and ethylene glycol

Zheng, Zubiao,Han, Bingbing,Wu, Fang,Shi, Tengfei,Liu, Jie,Zhang, Yong,Hao, Jialong

, p. 7738 - 7743 (2016/11/17)

A new process that could directly prepare α-haloacetal of ketones from various ketones with N-halosuccinimide (NBS/NCS) and ethylene glycol in one step without any other catalysts was reported. The effects of solvents, NBS/NCS and reaction temperature were investigated. Under the optimal condition, most of α-haloacetals of ketones were obtained in 90–100% yield.

STEREOCHEMICAL STUDIES-XXVI CONFORMATIONAL EQUILIBRIA OF KETALS OF 2-SUBSTITUTED CYCLOHEXANONES

Mursakulov, Ismail G.,Guseinov, M. M.,Kasumov, N. K.,Zefirov, Nikolai S.,Samoshin, V. V.,Chalenko, E. G.

, p. 2213 - 2220 (2007/10/02)

The positions of the conformational equilibria in a series of 2-substituted cyclohexanone ketals have been determined by 1H NMR.For the ethylene ketals 6 the equatorial conformer has been found to be enthalpically preferred.The other ketal syst

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