Welcome to LookChem.com Sign In|Join Free

CAS

  • or

1025892-26-5

1025892-26-5

Post Buying Request

1025892-26-5 Suppliers

Recommended suppliersmore

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

1025892-26-5 Usage

Uses

Intermediate in the production of labelled Cephalexin.

Check Digit Verification of cas no

The CAS Registry Mumber 1025892-26-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,5,8,9 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1025892-26:
(9*1)+(8*0)+(7*2)+(6*5)+(5*8)+(4*9)+(3*2)+(2*2)+(1*6)=145
145 % 10 = 5
So 1025892-26-5 is a valid CAS Registry Number.

1025892-26-5SDS

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 ethyl 2-oxo-2-(2,3,4,5,6-pentadeuteriophenyl)acetate

1.2 Other means of identification

Product number -
Other names Ethyl Benzoylformate-d5

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:1025892-26-5 SDS

1025892-26-5Relevant articles and documents

Ir(III)-Catalyzed Oxidative Annulation of Phenylglyoxylic Acids with Benzo[ b]thiophenes

Wang, Zhigang,Yang, Mufan,Yang, Yudong

, p. 3001 - 3005 (2018)

An Ir(III)-catalyzed oxidative annulation of phenylglyoxylic acids with benzo[b]thiophenes for the construction of benzothieno[3,2-c][2]benzopyranones in one step is disclosed. Three C-H cleavages and C-C/C-O bond formations are involved in this reaction. This protocol features a relatively broad substrate scope, good functional group tolerance, good regioselectivities, mild reaction conditions, and scale-up synthesis.

Controlled meta-Selective C-H Mono- And Di-Olefination of Mandelic Acid Derivatives

Muthuraja, Perumal,Usman, Rahamdil,Sajeev, Revathy,Gopinath, Purushothaman

supporting information, p. 6014 - 6018 (2021/08/03)

Mandelic acids represent a key structural motif present in many drug molecules. Herein, we report the controlled meta-selective mono- and diolefination of mandelic acids by the careful design of the substrate and oxidant. Furthermore, free meta-functional

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

What can I do for you?
Get Best Price

Get Best Price for 1025892-26-5