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136949-58-1

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136949-58-1 Usage

Chemical Properties

White to Off-White Solid

Uses

Diagnostic aid (radiopaque medium).

Definition

ChEBI: A benzenedicarboxamide compound having N-substituted carbamoyl groups at the 1- and 3-positions, iodo substituents at the 2-, 4- and 6-positions and a 3-hydroxy-2-(hydroxymethyl)propanimido at position 5.

Check Digit Verification of cas no

The CAS Registry Mumber 136949-58-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,9,4 and 9 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 136949-58:
(8*1)+(7*3)+(6*6)+(5*9)+(4*4)+(3*9)+(2*5)+(1*8)=171
171 % 10 = 1
So 136949-58-1 is a valid CAS Registry Number.
InChI:InChI=1/C20H28I3N3O9/c1-25(3-10(31)7-29)19(34)12-14(21)13(20(35)26(2)4-11(32)8-30)16(23)17(15(12)22)24-18(33)9(5-27)6-28/h9-11,27-32H,3-8H2,1-2H3,(H,24,33)

136949-58-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name iobitridol

1.2 Other means of identification

Product number -
Other names Xenetix

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:136949-58-1 SDS

136949-58-1Downstream Products

136949-58-1Relevant articles and documents

Iobitridol preparation method and iobitridol intermediate and preparation method thereof

-

, (2020/04/02)

The invention discloses an iobitridol preparation method and an iobitridol intermediate and a preparation method thereof, and specifically relates to an intermediate M1 5-(2-isopropyl-1,3-dioxane-5-carbonylacyl)-2,4,6-triiodo isophthalic acid for preparing iobitridol. The invention also discloses a preparation method of the intermediate M1 and a method for preparing iobitridol from the intermediate M1. The intermediate is high in activity and easy to prepare, and the method for synthesizing iobitridol from the intermediate is short in time, simple in synthesis method, low in comprehensive costand high in the yield and the purity of the reaction target object, and is suitable for industrial production.

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