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149883-42-1

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149883-42-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 149883-42-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,8,8 and 3 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 149883-42:
(8*1)+(7*4)+(6*9)+(5*8)+(4*8)+(3*3)+(2*4)+(1*2)=181
181 % 10 = 1
So 149883-42-1 is a valid CAS Registry Number.

149883-42-1SDS

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 8-O-demethylpseurotin A

1.2 Other means of identification

Product number -
Other names pseurotin A

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:149883-42-1 SDS

149883-42-1Upstream product

149883-42-1Downstream Products

149883-42-1Relevant articles and documents

Total syntheses of natural pseurotins A and F2 and azaspirene

Aoki, Shin-Ya,Oi, Takahiro,Shimizu, Kazuya,Shiraki, Ryota,Takao, Ken-Ichi,Tadano, Kin-Ichi

, p. 161 - 166 (2007/10/03)

Total syntheses of natural pseurotins A (1) and F2 (8-O-demethylpseurotin A) (2) and structurally related azaspirene (3), each possessing a novel heterospirocyclic system, i.e., 1-oxa-7-azaspiro[4.4]non-2-ene-4,6-dione skeleton, have been accom

Asymmetric total synthesis of pseurotin A

Hayashi, Yujiro,Shoji, Mitsuru,Yamaguchi, Shinpei,Mukaiyama, Takasuke,Yamaguchi, Junichiro,Kakeya, Hideaki,Osada, Hiroyuki

, p. 2287 - 2290 (2007/10/03)

(Matrix presented) The asymmetric total syntheses of pseurotin A and 8-O-demethylpseurotin A have been accomplished. Key reactions are a NaH-promoted intramolecular cyclization of an alkynylamide to form a γ-lactam, an aldol reaction of a benzylidene-subs

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