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88206-84-2

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88206-84-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88206-84-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,2,0 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 88206-84:
(7*8)+(6*8)+(5*2)+(4*0)+(3*6)+(2*8)+(1*4)=152
152 % 10 = 2
So 88206-84-2 is a valid CAS Registry Number.

88206-84-2SDS

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 hosenkol A

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

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:88206-84-2 SDS

88206-84-2Downstream Products

88206-84-2Relevant academic research and scientific papers

Hosenkosides A, B, C, D, and E, Novel Baccharane Glycosides from the Seeds of Impatiens balsamina

Shoji, Noboru,Umeyama, Akemi,Saitou, Nobuaki,Yoshikawa, Kazuko,Kan, Yukiko,Arihara, Shigenobu

, p. 4973 - 4986 (1994)

From the seeds of Impatiens balsamina has been isolated five novel baccharane glycosides, hosenkosides A-E.The structure of all isolates were secured by the use of 2D NMR techniques (1H-1H COSY, HMQC, HMBC, ROESY, TOCSY), CD spectroscopy and chemical derivatization.

Hosenkosides F, G, H, I, J, and K, novel baccharane glycosides from the seeds of Impatiens balsamina

Shoji,Umeyama,Saitou,Yoshikawa,Nagai,Arihara

, p. 1422 - 1426 (2007/10/02)

From the seeds of Impatiens balsamina we have isolated six novel baccharane glycosides, hosenkosides F-K. The structures of all isolates were determined by the use of two dimensional (2D) NMR techniques (1H-1H correlation spectroscopy (COSY), heteronuclear multiple quantum coherence (HMQC), heteronuclear multiple-bond correlation (HMBC), rotating frame Overhauser enhancement spectroscopy (ROESY), total correlation spectroscopy (TOCSY)) and chemical derivatization. Hosenkosides F, H and I are hosenkol B 3-O-sambubiosido-26-O-glucoside, 3-O-sambubioside and 3,26-O-diglucoside, respectively. Hosenkoside G is hosenkol C 3-O-sambubiosido-28-O-glucoside. Hosenkosides J and K are hosenkol A 3-O-sophoroside and 3-O-sophorosido-26- O-glucosyl-28-O-glucoside, respectively.

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