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86544-11-8

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86544-11-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86544-11-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,5,4 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 86544-11:
(7*8)+(6*6)+(5*5)+(4*4)+(3*4)+(2*1)+(1*1)=148
148 % 10 = 8
So 86544-11-8 is a valid CAS Registry Number.

86544-11-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-hydroxy-6-methoxy-6-oxohexanoate

1.2 Other means of identification

Product number -
Other names methyl 5-carboxy-2-hydroxypentanoate

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:86544-11-8 SDS

86544-11-8Downstream Products

86544-11-8Relevant articles and documents

DYE-SENSITIZED PHOTO-OXYGENATION OF 1,2-CYCLOHEXANEDIONES

Utaka, Masanori,Nakatani, Manabu,Takeda, Akira

, p. 2163 - 2168 (2007/10/02)

The dye-sensitized photo-oxygenation of the enols of 1,2-cyclohexanedione (1) has been carried out in various solvents at -70 - 40 deg C.Singlet oxygen is involved in the reaction as evidenced by quenching and rate enhancement observed in deuterated methanol.The reaction proceeds by an ene reaction with singlet oxygen to afford the hydroperoxide, 4, which closes to a five-membered endoperoxide, 5, as a major path or to dioxetane (6) as a minor one.The endoperoxide, 5, decomposed to 5-oxoalkanoic acid (2) with evolution of carbon monoxide or was trapped by the solvent (MeOH or EtOH) to give methyl or ethyl 5-carboxy-2-hydroxypentanoate (3).Competition between the enol of 3-methyl-1,2-cyclohexanedione (1a) and 2,3-dimethyl-2-butene (TME) has shown that the enol is as reactive as TME toward singlet oxygen.

PHOTOSENSITIZED OXYGENATION OF THE ENOL FORMS OF 1,2-CYCLOHEXANEDIONES

Utaka, Masanori,Nakatani, Manabu,Takeda, Akira

, p. 803 - 806 (2007/10/02)

The enols of 1,2-cyclohexanediones have been found to undergo a photosensitized oxygenation in methanol to afford 5-oxoalkanoic acids and methyl 5-carboxy-2-hydroxypentanoates with liberation of carbon monoxide with a remarkable temperature dependency of the product distribution, which is best accounted for in terms of trapping of a five-membered endoperoxide intermediate by methanol.

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