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7aH-Oxazolo[2,3-b]oxazole,tetrahydro-7a-(methoxymethyl)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

700724-95-4

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700724-95-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 700724-95-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,0,0,7,2 and 4 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 700724-95:
(8*7)+(7*0)+(6*0)+(5*7)+(4*2)+(3*4)+(2*9)+(1*5)=134
134 % 10 = 4
So 700724-95-4 is a valid CAS Registry Number.

700724-95-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 7a-(Methoxymethyl)tetrahydro[1,3]oxazolo[2,3-b][1,3]oxazole

1.2 Other means of identification

Product number -
Other names -

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:700724-95-4 SDS

700724-95-4Downstream Products

700724-95-4Relevant academic research and scientific papers

Preparation and characterization of bicyclic amide acetals and monothioacetals

Guthrie, J. Peter,Gallant, Roger T.,Jennings, Michael C.

, p. 268 - 278 (2007/10/03)

We have prepared and characterized new examples of 5-substituted-1-aza-4,6- dioxabicyclo[3.3.0]octanes (bicyclic amide acetals) and examples of the new heterocyclic system, 5-substituted-1-aza-4-oxa-6-thiabicyclo[3.3.0]octanes (bicyclic amide monothioacetals). Detailed analysis of NMR coupling constants and X-ray structure determination for an example of each class of compound established the stereochemistry and conformation of these ring systems.

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