Welcome to LookChem.com Sign In|Join Free
  • or
Benzene, (azidomethoxymethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

127700-29-2

Post Buying Request

127700-29-2 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

127700-29-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127700-29-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,7,0 and 0 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 127700-29:
(8*1)+(7*2)+(6*7)+(5*7)+(4*0)+(3*0)+(2*2)+(1*9)=112
112 % 10 = 2
So 127700-29-2 is a valid CAS Registry Number.

127700-29-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name diazonio(phenylmethoxymethyl)azanide

1.2 Other means of identification

Product number -
Other names Azidomethoxyphenylmethane

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:127700-29-2 SDS

127700-29-2Upstream product

127700-29-2Relevant academic research and scientific papers

Indium(III) triflate catalyzed tandem azidation/1,3-dipolar cycloaddition reaction of ω,ω-dialkoxyalkyne derivatives with trimethylsilyl azide

Yanai, Hikaru,Taguchi, Takeo

, p. 8639 - 8643 (2005)

The azidation reaction of dialkyl acetal derivatives with trimethylsilyl azide (TMSN3) was efficiently catalyzed by 1-5 mol % of In(OTf) 3. The major product differed depending on the substrate structure and molar ratio of TMSN3

CONVERSION OF ACETALS INTO MONOTHIOACETALS, α-ALKOXYAZIDES AND α-ALKOXYALKYL THIOACETATES WITH MAGNESIUM BROMIDE

Kim, Sunggak,Park, Jung Ho,Lee, Sangphil

, p. 6697 - 6700 (2007/10/02)

Magnesium bromide in ether has been found to be a very mild and highly efficient reagent for the conversion of acetals into the corresponding monothioacetals, α-alkoxyazides and α-alkoxyalkyl thioacetates.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 127700-29-2