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Apoxocamphor, also known as apocamphor or apocamphore, is a synthetic organic compound derived from camphor. It is a white crystalline substance with a strong, pungent odor, and it is used as a fragrance ingredient in various products such as perfumes, soaps, and cosmetics. Apoxocamphor is also known for its insect-repellent properties, making it a popular ingredient in mosquito repellents and other insect control products. Additionally, it has been used in some pharmaceutical applications, such as in the treatment of respiratory conditions due to its expectorant and bronchodilator effects. However, it is important to note that the use of apocamphor in certain applications may be restricted or regulated due to potential health concerns, and it is always recommended to follow safety guidelines and regulations when handling or using this chemical.

6004-71-3

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6004-71-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6004-71-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,0 and 4 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6004-71:
(6*6)+(5*0)+(4*0)+(3*4)+(2*7)+(1*1)=63
63 % 10 = 3
So 6004-71-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H14O2/c1-9(2)7-3-4-10(9,6-11)8(12)5-7/h6-7H,3-5H2,1-2H3

6004-71-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 7,7-dimethyl-3-oxobicyclo[2.2.1]heptane-4-carbaldehyde

1.2 Other means of identification

Product number -
Other names Apocamphor-1-carboxaldehyde

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:6004-71-3 SDS

6004-71-3Downstream Products

6004-71-3Relevant academic research and scientific papers

Radical Chain Reaction or Benzenethiol with Pentynylthiol Esters: Production of Aldehydes under Stannane/Silane-Free Conditions

Benati, Luisa,Leardini, Rino,Minozzi, Matteo,Nanni, Daniele,Scialpi, Rosanna,Spagnolo, Piero,Zanardi, Giuseppe

, p. 985 - 990 (2007/10/03)

The radical chain reaction of benzenethiol with accessible 4-pentynylthiol esters provides a new stannane/silane-free protocol for the production of aromatic and aliphatic aldehydes. The procedure is especially useful for the aryl and primary aldehydes, even in the presence of substituents highly sensitive to reductive conditions, and is also of some utility for the vinylic and secondary ones, The protocol is instead not applicable to the tertiary aldehydes, owing to preferential alkane-forming decarbonylation, although the tertiary ones derived from bridgehead precursors can still be usefully produced.

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