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6346-00-5

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6346-00-5 Usage

Physical state

Colorless liquid

Odor

Slightly sweet

Solubility

Soluble in water

Specific content

Commonly used as a fragrance ingredient in cosmetic and personal care products
Used in the manufacturing of pharmaceuticals and other industrial products
Utilized as a solvent and a chemical intermediate
Has antimicrobial properties and used in some disinfectant products

Check Digit Verification of cas no

The CAS Registry Mumber 6346-00-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,4 and 6 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6346-00:
(6*6)+(5*3)+(4*4)+(3*6)+(2*0)+(1*0)=85
85 % 10 = 5
So 6346-00-5 is a valid CAS Registry Number.

6346-00-5Relevant articles and documents

A synthesis method of diol

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Paragraph 0025-0030, (2022/01/12)

The present invention belongs to the field of organic synthesis technology, specifically a synthesis method of a diol; the present invention by bis (trimethylsilyl) lithium amino catalytic lactone boronization of lactone to synthesize a variety of structure of the diol compound; specifically, under the bis (trimethylsilyl) amino lithium catalytic system, to a variety of lactone compounds and pinacol borane as raw materials, the preparation of diol compounds; the method of the present invention raw materials are of a wide range of sources or easy to prepare, easy to operate, selective and controllable, high yield, mild conditions, universality wide.

A phosphine-free iron complex-catalyzed synthesis of cycloalkanes: Via the borrowing hydrogen strategy

Bettoni, Léo,Gaillard, Sylvain,Renaud, Jean-Luc

supporting information, p. 12909 - 12912 (2020/11/07)

Herein we report a diaminocyclopentadienone iron tricarbonyl complex catalyzed synthesis of substituted cyclopentane, cyclohexane and cycloheptane compounds using the borrowing hydrogen strategy in the presence of various substituted primary and secondary 1,n diols as alkylating reagents. Deuterium labeling experiments confirm that the diols were the hydride source in this cascade process. This journal is

Stereoselective synthesis of alicyclic ketones: A hydrogen borrowing approach

Armstrong, Roly J.,Akhtar, Wasim M.,Frost, James R.,Christensen, Kirsten E.,Stevenson, Neil G.,Donohoe, Timothy J.

supporting information, (2019/11/13)

A highly diastereoselective annulation strategy for the synthesis of alicyclic ketones from diols and pentamethylacetophenone is described. This process is mediated by a commercially available iridium(III) catalyst, and provides efficient access to a wide range of cyclopentane and cyclohexane products with high levels of stereoselectivity. The origins of diastereoselectivity in the annulation reaction have been explored by a series of control experiments, which provides an explanation for how each stereocentre around the newly forged ring is controlled.

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