Welcome to LookChem.com Sign In|Join Free

CAS

  • or

1900-69-2

Post Buying Request

1900-69-2 Suppliers

Recommended suppliersmore

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

1900-69-2 Usage

General Description

Trans-4-tert-butylcyclohexyl acetate is a chemical compound commonly used in the fragrance and flavor industry. It is a colorless liquid with a sweet, fruity aroma and is often used as a flavoring agent in food products and as a fragrance ingredient in perfumes, soaps, and other cosmetics. It is also used as a solvent in some industrial applications. This chemical is considered relatively safe for use in consumer products and has low toxicity. However, it should still be handled with care and in accordance with safety guidelines to prevent potential health or environmental hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 1900-69-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,0 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1900-69:
(6*1)+(5*9)+(4*0)+(3*0)+(2*6)+(1*9)=72
72 % 10 = 2
So 1900-69-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H22O2/c1-9(13)14-11-7-5-10(6-8-11)12(2,3)4/h10-11H,5-8H2,1-4H3/t10-,11-

1900-69-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name acetoxy-1 t-butyl-4 cyclohexane trans

1.2 Other means of identification

Product number -
Other names trans-Acetoxy-4-tert-butylcyclohexane

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:1900-69-2 SDS

1900-69-2Relevant articles and documents

Trans-Selective and Switchable Arene Hydrogenation of Phenol Derivatives

Bergander, Klaus,Glorius, Frank,Heusler, Arne,Wollenburg, Marco

, p. 11365 - 11370 (2020/11/24)

A trans-selective arene hydrogenation of abundant phenol derivatives catalyzed by a commercially available heterogeneous palladium catalyst is reported. The described method tolerates a variety of functional groups and provides access to a broad scope of trans-configurated cyclohexanols as potential building blocks for life sciences and beyond in a one-step procedure. The transformation is strategically important because arene hydrogenation preferentially delivers the opposite cis-isomers. The diastereoselectivity of the phenol hydrogenation can be switched to the cis-isomers by employing rhodium-based catalysts. Moreover, a protocol for the chemoselective hydrogenation of phenols to cyclohexanones was developed.

2-Norbornanediazonium Ions Revisited

Kirmse, Wolfgang,Siegfried, Rainer

, p. 950 - 956 (2007/10/02)

The reactions of 2-norbornanediazonium ions have been reinvestigated with the aid of optically active and deuterium-labeled precursors.Enantiomeric purities were determined by direct VPC methods, and deuterium distributions by 2H NMR spectroscopy.The product pattern is strongly affected by the polarity of the solvent. exo-Diazonium ions 13 in water yield racemic exo alcohol (s,kΔ) of the norbornadiazonium ions.Optically active exo products are typical of nonpolar solvents and originate most probably from assymetric ion pairs.Model studies with optically active bicyclooct-3-en-2-amine (36) provide conclusive evidence that ion-pair colapse may lead to optically active products even in the case of delocalized achiral carbocations.

Acid-induced 13C Nuclear Magnetic Resonance Chemical Shift Changes of Ether and Ester Carbon Atoms

Begtrup, Mikael

, p. 1609 - 1618 (2007/10/02)

13C N.m.r. chemical shifts of ehters dissolved in tetrachloromethane are displaced on addition of trifluoroacetic acid.The displacements result from independent interactions of the acid with the substrate oxygen atoms and alkyl residues.The structure-dependent and stereoselective shift changes are useful for signal assignments, structure determination, conformational analysis, assessment of the distribution of rapidly interconverting conformers of esters, and estimation of the relative basicity of ethers.

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 1900-69-2