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3-(3,7-dimethylocta-2,6-dien-1-yl)-4-hydroxybenzoic acid is a complex organic compound with the molecular formula C16H22O3. It is characterized by a benzoic acid structure, which includes a benzene ring with a hydroxyl group at the 4-position and a carboxyl group at the 1-position. The compound is further distinguished by the presence of a 3,7-dimethylocta-2,6-dien-1-yl group attached to the 3-position of the benzene ring. This group consists of an octadiene chain with two methyl groups at the 3 and 7 positions, respectively. The compound is known for its potential applications in various chemical and pharmaceutical industries, particularly as an intermediate in the synthesis of certain pharmaceuticals and natural products. Its unique structure and functional groups make it an interesting target for chemical research and development.

6917-57-3

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6917-57-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6917-57-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,1 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6917-57:
(6*6)+(5*9)+(4*1)+(3*7)+(2*5)+(1*7)=123
123 % 10 = 3
So 6917-57-3 is a valid CAS Registry Number.

6917-57-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(3,7-dimethylocta-2,6-dienyl)-4-hydroxybenzoic acid

1.2 Other means of identification

Product number -
Other names -

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

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More Details:6917-57-3 SDS

6917-57-3Upstream product

6917-57-3Downstream Products

6917-57-3Relevant academic research and scientific papers

Sodium hydridotrimethylboronate and its ether solvate. Study of hydridotrialkylboronates as reagents for the preparation of beryllium hydrides

Bell, Norman A.,Coates, Geoffrey E.,Heslop, J. Alan

, p. 287 - 292 (2007/10/02)

Sodium hydridotrimethylborate is tetrameric in benzene solution and its etherate, (NaBMe3H)4OEt2 probably also retains its solid state cubane arrangement in benzene solution.Reactions of NaBR3H (R = Me, Et) in a variety of ratios with halo and organoberyllium compounds have been studied.Exchange between Et2Be and NaBEt3H does not occur to any appreciable extent beyond the EtBH stage and reaction of equimolar EtBeCl and NaBEt3H resulted in the formation of EtBeH, isolated as its trimethylamine complex.NaBR3H and BeCl2 in 1/1, 2/1 and 4/1 ratios did not yield pure beryllium hydrides.

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