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14064-39-2 Usage

General Description

L-Galactose, 6-deoxy-3-O-methyl- is a chemical compound that is a derivative of the sugar galactose. It is characterized by the presence of a methyl group at the third position and a deoxy group at the sixth position of the galactose molecule. L-Galactose, 6-deoxy-3-O-methyl- has potential applications in the pharmaceutical and food industries, as it has been shown to possess antimicrobial and antioxidant properties. Additionally, L-Galactose, 6-deoxy-3-O-methyl- may have potential therapeutic applications in the treatment of certain diseases, as it has been found to exhibit anti-inflammatory and immunomodulatory effects. Overall, this compound shows promise for various biomedical and industrial applications due to its unique chemical structure and potential beneficial properties.

Check Digit Verification of cas no

The CAS Registry Mumber 14064-39-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,0,6 and 4 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 14064-39:
82 % 10 = 2
So 14064-39-2 is a valid CAS Registry Number.



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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017


1.1 GHS Product identifier

Product name (2S,3R,4R,5S)-2,4,5-trihydroxy-3-methoxyhexanal

1.2 Other means of identification

Product number -
Other names L-Galactose,6-deoxy-3-O-methyl

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:14064-39-2 SDS

14064-39-2Relevant articles and documents

Four new pregnane glycosides from Gymnema latifolium and their α-glucosidase and α-amylase inhibitory activities

Yen, Duong Thi Hai,Trang, Do Thi,Tai, Bui Huu,Doan, Vu Van,Yen, Pham Hai,Nhiem, Nguyen Xuan,Van Minh, Chau,Hoang Duc, Manh,Park, SeonJu,Hyuk Lee, Jae,Kim, Sun Yeou,Kim, Seung Hyun,Kiem, Phan Van

supporting information, p. 4460 - 4467 (2020/03/03)

Four new pregnane glycosides, gymlatifosides A - D (1 ? 4) and one known pregnane glycoside, verticilloside J (5) were isolated from the leaves of Gymnema latifolium Wall. ex Wight. Their chemical structures were elucidated on the basis of extensive spectroscopic methods, including 1D, 2D NMR, HR-ESI-MS, and in comparison with the reported data. All these compounds were tested for α-glucosidase and α-amylase inhibitory activities. Compound 5 exhibited the most anti α-glucosidase activity with inhibitory percentage of 37.8 ± 1.5% at the concentration of 200 μM. Compounds 1–4 showed moderate anti α-glucosidase activity with inhibitory percentage ranging from 7.0 to 30.1%. In addition, all compounds 1–5 showed moderate/weak anti α-amylase activity in the investigated test.

Melanogenesis inhibitory pregnane glycosides from Cynanchum atratum

Jin, Qinghao,Han, Xiang Hua,Yun, Cheong-Yong,Lee, Chul,Lee, Jin Woo,Lee, Dongho,Lee, Mi Kyeong,Jung, Sang-Hun,Hong, Jin Tae,Kim, Youngsoo,Hwang, Bang Yeon

supporting information, p. 1252 - 1256 (2018/03/12)

Bioassay-guided fractionation of the methanolic extract from the roots of Cynanchum atratum has resulted in the isolation of three new pregnane glycosides (1–3) along with four known compounds (4–7). Their structures were identified by analysis of the spectroscopic data including extensive 2D NMR. All of the isolates were evaluated for their potential to inhibit the melanin production in α-melanocyte stimulating hormone (α-MSH)-activated B16 melanoma cells. Of these, compounds 4–7 dose-dependently inhibited the melanin production with the IC50 values ranging from 4 μM to 33 μM.

New C21 steroidal glycosides from the roots of Cynanchum stauntonii and their protective effects on hypoxia/reoxygenation induced cardiomyocyte injury

Lei, Qiao-Shi,Zuo, Yi-Han,Lai, Chang-Zhi,Luo, Jin-Fang,Pang, Shu-Wen,Zhou, Hua,Yao, Xin-Sheng,Tang, Jin-Shan

, p. 1716 - 1722 (2017/07/27)

Phytochemical investigations from the roots of Cynanchum stauntonii led to obtain four new C21 steroidal glycosides (1–4) and one known compound stauntoside F (5). Their chemical structures were characterized by sophisticated analyses of IR, HR

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