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4,5-Octanedione, 3,6-bis(1,1-dimethylethyl)-2,2,7,7-tetramethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

29679-00-3

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29679-00-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29679-00-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,6,7 and 9 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 29679-00:
(7*2)+(6*9)+(5*6)+(4*7)+(3*9)+(2*0)+(1*0)=153
153 % 10 = 3
So 29679-00-3 is a valid CAS Registry Number.

29679-00-3SDS

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 3,6-di-tert-butyl-2,2,7,7-tetramethyl-octane-4,5-dione

1.2 Other means of identification

Product number -
Other names 2,2,7,7-tetramethyl-3,6-di-tert-butyl-4,5-octanedione

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:29679-00-3 SDS

29679-00-3Downstream Products

29679-00-3Relevant academic research and scientific papers

Photochemical Behavior of Thioketenes in Solution: Reaction from S2

Singh, Sharat,Nimmesgern, Hildegard,Schaumann, Ernst,Ramamurthy, Vaidhyanathan

, p. 4799 - 4805 (2007/10/02)

The higher excited-state reactions of sterically encumbered thioketenes 1a-d in solution were investigated.Substituted thiiranes, thio esters, thioacetophenones, and 1,2-diones are formed on photoexcitation of thioketenes in hydroxylic and nonhydroxylic solvents.Thioketenes while unreactive upon excitation to S1 produce thiiranylidene carbene and zwitterionic intermediates upon excitation to S2.The reactive state is identified to be S2 (??*).The excited thioketene resists carbon monosulfide elimination but undergoes rearrangement.The photobehavior of thioketenes, established in solution for the first time, differs significantly from that of ketenes, and it cannot be extrapolated from that of structurally analogous ketenes and allenes.

Upper Excited State Reactions of Thioketenes: Di-tert-butylthioketene

Singh, Sharat,Ramamurthy, V.

, p. 393 - 395 (2007/10/02)

Di-tert-butylthioketene, while unreactive upon excitation to S1, produces thiirenylidene carbene and zwitterionic intermediates upon excitation to S2.

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