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7299-40-3

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7299-40-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7299-40-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,9 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7299-40:
(6*7)+(5*2)+(4*9)+(3*9)+(2*4)+(1*0)=123
123 % 10 = 3
So 7299-40-3 is a valid CAS Registry Number.

7299-40-3SDS

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 (r-l,t-4)-p-menth-8-en-1-ol

1.2 Other means of identification

Product number -
Other names β-cis-terpineol

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:7299-40-3 SDS

7299-40-3Relevant articles and documents

Synthesis of Terpineol from Alpha-Pinene Catalyzed by α-Hydroxy Acids

Hu, Yi-Ming,Huang, Xiao-Rui,Meng, Zhong-Lei,Qin, Rong-Xiu,Wen, Ru-Si,Zhou, Yong-Hong

, (2022/02/17)

We report the use of five alpha-hydroxy acids (citric, tartaric, mandelic, lactic and glycolic acids) as catalysts in the synthesis of terpineol from alpha-pinene. The study found that the hydration rate of pinene was slow when only catalyzed by alpha-hydroxyl acids. Ternary composite catalysts, composed of AHAs, phosphoric acid, and acetic acid, had a good catalytic performance. The reaction step was hydrolysis of the intermediate terpinyl acetate, which yielded terpineol. The optimal reaction conditions were as follows: alpha-pinene, acetic acid, water, citric acid, and phosphoric acid, at a mass ratio of 1:2.5:1:(0.1–0.05):0.05, a reaction temperature of 70? C, and a reaction time of 12–15 h. The conversion of alpha-pinene was 96%, the content of alpha-terpineol was 46.9%, and the selectivity of alpha-terpineol was 48.1%. In addition, the catalytic performance of monolayer graphene oxide and its composite catalyst with citric acid was studied, with acetic acid used as an additive.

Organometallic Mo complex anchored to magnetic iron oxide nanoparticles as highly recyclable epoxidation catalyst Dedicated to Prof. Maria José Calhorda on the occasion of her 65th birthday

Fernandes, Cristina I.,Carvalho, Maria Deus,Ferreira, Liliana P.,Nunes, Carla D.,Vaz, Pedro D.

, p. 2 - 10 (2014/05/06)

The organometallic fragment [MoI2(CO)3] was coordinated to magnetic iron oxide nanoparticles of different sizes (average size of 11 and 30 nm) which have been previously coated with a silica shell and grafted with a pyridine derivative ligand. The Mo loading was found to be approximately 0.37 wt-% Mo and 0.57 wt-% Mo, corresponding to 0.150 mmol Mo g-1 and 0.230 mmolMo g-1 for materials MNP30-Si-inic-Mo and MNP11-Si-inic-Mo, respectively. Preparation of these organometallic decorated magnetic nanoparticles was further confirmed by evidence obtained from extensive characterization by powder XRD, SEM/TEM analysis, as well as from data of 57Fe M?ssbauer and FTIR spectroscopy. Olefin epoxidation of a variety of substrates promoted by these organometallic nano-hybrid materials using tbhp as oxidant, was performed with very good results. The catalytic studies show that the catalysts yield selectively the desired epoxides of a series of olefins. In addition, these catalysts are found to work under a wide temperature range and over several catalytic cycles without notorious performance loss in most cases.

Monoterpene hydroperoxides with trypanocidal activity from Chenopodium ambrosioides

Kiuchi, Fumiyuki,Itano, Yoshiaki,Uchiyama, Nahoko,Honda, Gisho,Tsubouchi, Akiko,Nakajima-Shimada, Junko,Aoki, Takashi

, p. 509 - 512 (2007/10/03)

Four monoterpene hydroperoxides were isolated from aerial parts of Chenopodium ambrosioides along with ascaridole (1), the anthelmintic principle of this plant, as anti-trypanosomal compounds. The structures of these monoterpenes were determined to be (-)

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