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1118786-87-0

1118786-87-0

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1118786-87-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1118786-87-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,1,8,7,8 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1118786-87:
(9*1)+(8*1)+(7*1)+(6*8)+(5*7)+(4*8)+(3*6)+(2*8)+(1*7)=180
180 % 10 = 0
So 1118786-87-0 is a valid CAS Registry Number.

1118786-87-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6,6-dimethoxy-spiro[3.3]heptane-2,2-dicarboxylic acid diisopropyl ester

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:1118786-87-0 SDS

1118786-87-0Relevant articles and documents

SPIRO COMPOUND AS INDOLEAMINE-2,3-DIOXYGENASE INHIBITOR

-

, (2020/12/29)

Disclosed in the present invention are an indoleamine-2,3-dioxygenase inhibitor and a preparation method therefor. The inhibitor of the present invention has a structure as represented by general formula (I), wherein the definitions of Ar, E, Y, X, V, D, W, B, ring A and ring B are as shown in the description and claims. Also disclosed in the present invention is a preparation method for the inhibitor. The compound of general formula (I) of the present invention can be used as an indoleamine-2,3-dioxygenase inhibitor for preparing a medicament for preventing and/or treating indoleamine-2,3-dioxygenase-mediated diseases.

Synthesis of conformationally restricted glutamic acid analogs based on the spiro[3.3]heptane scaffold

Radchenko, Dmytro S.,Grygorenko, Oleksandr O.,Komarov, Igor V.

experimental part, p. 2924 - 2930 (2009/07/04)

A library of isomeric glutamic acid analogs based on the spiro[3.3]heptane skeleton is designed. Two members of the library, (R)- and (S)-2-amino-spiro[3.3]heptane-2,6-dicarboxylic acid hydrochlorides, were synthesized. The stereochemistry of the synthesi

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