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126399-11-9

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126399-11-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126399-11-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,3,9 and 9 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 126399-11:
(8*1)+(7*2)+(6*6)+(5*3)+(4*9)+(3*9)+(2*1)+(1*1)=139
139 % 10 = 9
So 126399-11-9 is a valid CAS Registry Number.

126399-11-9SDS

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 (2S,3S,4E)-6-bromo-2-methoxy-3,5-dimethyl-1-phenyl-4-hexene

1.2 Other means of identification

Product number -
Other names ((E)-(2S,3S)-6-Bromo-2-methoxy-3,5-dimethyl-hex-4-enyl)-benzene

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:126399-11-9 SDS

126399-11-9Downstream Products

126399-11-9Relevant articles and documents

Total synthesis of motuporin (nodularin-v)

Bauer, Shawn M.,Armstrong, Robert W.

, p. 6355 - 6366 (2007/10/03)

The serine/threonine phosphatase (protein phosphatase 1 and 2A) inhibitors constitute a biologically and structurally interesting class of natural products. Among this class of inhibitors are cyclic pentapeptides (nodularins) and cyclic heptapeptides (mic

Stereocontrolled Synthesis of (2S,3S,8S,9S,4E,6E)-3-Amino-9-methoxy-2,6,8-trimethyl-10-phenyldeca-4,6-dienoic Acid (Adda), the Amino Acid Characteristic of Microcystins and Nodularin

Beatty, Mark F.,Jennings-White, Clive,Avery, Mitchell A.

, p. 1637 - 1642 (2007/10/02)

(4R,5S)-4-Methyl-5-phenyloxazolidin-2-one has been used as a chiral template to construct the 8S and 9S chiral centres of (2S,3S,8S,9S)-3-amino-9-methoxy-2,6,8-trimethyl-10-phenyldeca-4,6-dienoic acid (Adda), the 2S and 3S centres being derived from D-asp

Total synthesis of N-phthaloyl adda methyl ester: All stereocenters originating from a single chiral epoxyalcohol

Chakraborty,Joshi

, p. 2043 - 2046 (2007/10/02)

Selective ring opening of (2S,3R)-epoxide of 4-benzyloxy-cis-2-buten-1-ol either at 2- or 3-position ensures stereospecific construction of all the chiral centers of Adda.

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