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741283-41-0

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741283-41-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 741283-41-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,1,2,8 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 741283-41:
(8*7)+(7*4)+(6*1)+(5*2)+(4*8)+(3*3)+(2*4)+(1*1)=150
150 % 10 = 0
So 741283-41-0 is a valid CAS Registry Number.

741283-41-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-iodo-2-methoxy-1-phenylmethoxybenzene

1.2 Other means of identification

Product number -
Other names 4-benzyloxy-1-iodo-3-methoxybenzene

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:741283-41-0 SDS

741283-41-0Relevant articles and documents

Three white lignan and simplify structure, its preparation process and its pharmaceutical composition and use thereof

-

, (2017/01/17)

Disclosed a saucernetin structurally simplified substance and the preparation method and pharmaceutical composition and use thereof. In particular, it relates to a compound of general formula (I) shown as formula (I) or an isomer thereof and a salt thereo

Synthesis of multiply 13C-labeled furofuran lignans using 13C-labeled cinnamyl alcohols as building blocks

Haajanen, Kati,Botting, Nigel P.

, p. 231 - 239 (2007/10/03)

Plant lignans are currently being widely studied for their potential benefits for human health as their consumption has been correlated with lower risks for developing chronic diseases, such as breast cancer and coronary heart disease. However, studies of

SYNTHESIS OF 13C-LABELLED ESTROGEN ANALOGUES

-

Page 25, (2010/02/08)

There is provided a method of producing novel 13C-labelled estrogen analogues. The method preferably proceeds via an intermediate A or B or which is a mixture of (A) or (B): wherein a13C atom is located at one or more of positions 1, 2, 3 or 4 and wherein R is an optionally substituted alkane, alkene, alkyne or aryl group. Preferably R is -CH2Ph. An alternative preferred intermediate compound is 13C-resorcinol.

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