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4060-08-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4060-08-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,6 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4060-08:
56 % 10 = 6
So 4060-08-6 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 20, 2017

Revision Date: Aug 20, 2017


1.1 GHS Product identifier

Product name 3-O-methyl-L-rhamnose

1.2 Other means of identification

Product number -
Other names O3-methyl-L-6-deoxy-mannose

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:4060-08-6 SDS

4060-08-6Relevant 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.

Cytotoxic Cardiac Glycoside Constituents of Vallaris glabra Leaves

Kruakaew, Sudarat,Seeka, Chonticha,Lhinhatrakool, Thitima,Thongnest, Sanit,Yahuafai, Jantana,Piyaviriyakul, Suratsawadee,Siripong, Pongpun,Sutthivaiyakit, Somyote

, p. 2987 - 2996 (2017/12/01)

Thirteen cardenolide glycosides (1-13) were isolated from the CH2Cl2 and MeOH extracts of Vallaris glabra leaves. The structures of the new compounds (2-13) were identified by spectroscopic methods, with the absolute configurations o

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