Welcome to LookChem.com Sign In|Join Free

CAS

  • or

38274-25-8

Post Buying Request

38274-25-8 Suppliers

Recommended suppliersmore

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

38274-25-8 Usage

General Description

1,4-BUTANEDIOL-2,2,3,3-D4 is a chemical compound that is a deuterated form of 1,4-butanediol, which is commonly used as a solvent and reagent in organic synthesis. The deuterated form, 2,2,3,3-D4, contains four deuterium atoms, which are heavy isotopes of hydrogen. 1,4-BUTANEDIOL-2,2,3,3-D4 is used in research and pharmaceutical applications as a labeled standard for mass spectrometry and nuclear magnetic resonance (NMR) spectroscopy. It is also used in the production of specialty chemicals and polymers. The presence of deuterium atoms can alter the physical and chemical properties of the compound, making it useful in studying reaction mechanisms and metabolic pathways.

Check Digit Verification of cas no

The CAS Registry Mumber 38274-25-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,2,7 and 4 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 38274-25:
(7*3)+(6*8)+(5*2)+(4*7)+(3*4)+(2*2)+(1*5)=128
128 % 10 = 8
So 38274-25-8 is a valid CAS Registry Number.

38274-25-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,3,3-tetradeuteriobutane-1,4-diol

1.2 Other means of identification

Product number -
Other names 2,2,3,3-tetradeuterio-butane-1,4-diol

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:38274-25-8 SDS

38274-25-8Upstream product

38274-25-8Relevant articles and documents

Formation of RuII-alkyl-butadiene complexes from dihalogeno-RuIV-allyl precursors by the reaction with BrMg(CH2)4MgBr: a novel decomposition pathway for ruthena(IV)cyclopentane intermediates

Nagashima, Hideo,Michino, Yoshiyuki,Ara, Ken-ichi,Fukahori, Takahiko,Itoh, Kenji

, p. 189 - 196 (2007/10/02)

Treatment of (C5Me5)RuBr2(η3-CH2C(R)CH2) with BrMg(CH2)4MgBr in ether afforded the RuII-alkyl-butadiene complexes, (C5Me5)Ru(η4-C4H6)(η1-Ch2CHRCH3) .Labeling experiments have revealed a mechanism involving a double β-hydrogen elimination from ruthenacyclopentane intermediates and subsequent stepwise transfer of the hydrogen atoms to hydrogenate the η3-allyl ligand.

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 38274-25-8